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    1. Ota, N; Nakajima, T; Nakazawa, I; Suzuki, T; Hosoi, T; Orimo, H; Inoue, S; Shirai, Y; Emi, M
      A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density

      JOURNAL OF HUMAN GENETICS
    2. Kishimoto, Y; Morisawa, T; Kitano, M; Shiota, G; Horie, Y; Suou, T; Ito, H; Kawasaki, H; Hasegawa, J
      Loss of heterozygosity of the mannose 6-phosphate/insulin-like growth factor II receptor and p53 genes in human hepatocellular carcinoma

      HEPATOLOGY RESEARCH
    3. Nakanishi, M; Tanaka, K; Takahashi, T; Kyo, T; Dohy, H; Fujiwara, M; Kamada, N
      Microsatellite instability in acute myelocytic leukaemia developed from A-bomb survivors

      INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
    4. Virgos, C; Martorell, L; Valero, J; Figuera, L; Civeira, F; Joven, J; Labad, A; Vilella, E
      Association study of schizophrenia with polymorphisms at six candidate genes

      SCHIZOPHRENIA RESEARCH
    5. Chen, HY; Chen, WC; Tsai, HD; Hsu, CD; Tsai, FJ; Tsai, CH
      Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan

      MATURITAS
    6. Scott, BT; Bovill, EG; Callas, PW; Hasstedt, SJ; Leppert, MF; Valliere, JE; Varvil, TS; Long, GL
      Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred

      THROMBOSIS AND HAEMOSTASIS
    7. Papadimitriou, G; Dikeos, D; Daskalopoulou, E; Karadima, G; Avramopoulos, D; Contis, C; Stefanis, C
      Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset

      NEUROPSYCHOBIOLOGY
    8. Eklund, LK; Islam, K; Soderkvist, P; Islam, MQ
      Regional mapping of suppressor loci for anchorage independence and tumorigenicity on human chromosome 9

      CANCER GENETICS AND CYTOGENETICS
    9. Sud, R; Wells, D; Talbot, IC; Delhanty, JDA
      Genetic alterations in gastric cancers from British patients

      CANCER GENETICS AND CYTOGENETICS
    10. Lee, KB; Kunugi, H; Nanko, S
      Glial cell line-derived neurotrophic factor (GDNF) gene and schizophrenia:polymorphism screening and association analysis

      PSYCHIATRY RESEARCH
    11. Smoller, JW; Rosenbaum, JF; Biederman, J; Susswein, LS; Kennedy, J; Kagan, J; Snidman, N; Laird, N; Tsuang, MT; Faraone, SV; Schwarz, A; Slaugenhaupt, SA
      Genetic association analysis of behavioral inhibition using candidate locifrom mouse models

      AMERICAN JOURNAL OF MEDICAL GENETICS
    12. Teraoka, M; Narahara, K; Yokoyama, Y; Ninomiya, S; Mizuta, S; Une, T; Seino, Y
      Maternal origin of a unique extra chromosome, der(9)(pter -> q13 :: q13 ->q12 :) in a girl with typical trisomy 9p syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    13. Arruga, MV; Monteagudo, LV; Tejedor, MT; Barrao, R; Ponz, R
      Analysis of microsatellites and paternity testing in Rasa Aragonesa sheep

      RESEARCH IN VETERINARY SCIENCE
    14. Mogensen, J; Andersen, PS; Steffensen, U; Christiansen, M; Egeblad, H; Gregersen, N; Borglum, AD
      Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy

      JOURNAL OF MEDICAL GENETICS
    15. Westberg, L; Baghaei, F; Rosmond, R; Hellstrand, M; Landen, M; Jansson, M; Holm, G; Bjorntorp, P; Erikson, E
      Polymorphisms of the androgen receptor gene and the estrogen receptor betagene are associated with androgen levels in women

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    16. Yashiro, M; Carethers, JM; Laghi, L; Saito, K; Slezak, P; Jaramillo, E; Rubio, C; Koizumi, K; Hirakawa, K; Boland, CR
      Genetic pathways in the evolution of morphologically distinct colorectal neoplasms

      CANCER RESEARCH
    17. Manga, P; Kromberg, JGR; Turner, A; Jenkins, T; Ramsay, M
      In southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified

      AMERICAN JOURNAL OF HUMAN GENETICS
    18. Glenn, BS; Stewart, WF; Schwartz, BS; Bressler, J
      Relation of alleles of the sodium-potassium adenosine triphosphatase alpha2 gene with blood pressure and lead exposure

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    19. Grubber, JM; Saunders, AM; Yamaoka, LH; Scott, WK; Martin, ER; Hill, DM; Standen, CL; Conneally, PM; Small, GW; Lai, EH; Gilbert, JR; Roses, AD; Haines, JL; Pericak-Vance, MA
      Analysis of chromosome 12 candidate genes in late-onset Alzheimer disease

      ALZHEIMERS REPORTS
    20. Ogawa, S; Emi, M; Shiraki, M; Hosoi, T; Ouchi, Y; Inoue, S
      Association of estrogen receptor beta (ESR2) gene polymorphism with blood pressure

      JOURNAL OF HUMAN GENETICS
    21. Thompson, JA; Chen, PL; King, RA; Rich, SS; Oetting, WS; Armstrong, C; Folsom, AR; Sellers, TA
      BRCA1 susceptibility markers and postmenopausal breast cancer: The Iowa Women's Health Study

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    22. Tabet-Aoul, K; Oustry-Vaiman, A; Vaiman, D; Saidi-Mehtar, N; Cribiu, EP; Lantier, F
      Cytogenetical anchoring of sheep linkage map and syntenic groups using a sheep BAC library

      GENETICS SELECTION EVOLUTION
    23. Brown, RL; Pollock, AN; Couchman, KG; Hodges, M; Hutchinson, DO; Waaka, R; Lynch, P; McCarthy, TV; Stowell, KM
      A novel ryanodine receptor mutation and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree

      HUMAN MOLECULAR GENETICS
    24. Slate, J; Marshall, T; Pemberton, J
      A retrospective assessment of the accuracy of the paternity inference program CERVUS

      MOLECULAR ECOLOGY
    25. Wendel, B; Reinhard, R; Wachtendorf, U; Zacharzowsky, UB; Osterziel, KJ; Schulte, HD; Haase, H; Hoehe, MR; Morano, I
      The human beta-myosin heavy chain gene: Sequence diversity and functional characteristics of the protein

      JOURNAL OF CELLULAR BIOCHEMISTRY
    26. Baptista, MJ; Fairbrother, UL; Howard, CM; Farrer, MJ; Davies, GE; Trikka, D; Maratou, K; Redington, A; Greve, G; Njolstad, PR; Kessling, AM
      Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

      HUMAN GENETICS
    27. Takagi, H; Ishiguro, N; Iwata, H; Kanamono, T
      Genetic association between rheumatoid arthritis and estrogen receptor microsatellite polymorphism

      JOURNAL OF RHEUMATOLOGY
    28. Uchida, A; Tachibana, M; Miyakawa, A; Nakamura, K; Mural, M
      Microsatellite analysis in multiple chromosomal regions as a prognostic indicator of primary bladder cancer

      UROLOGICAL RESEARCH
    29. Handel-Fernandez, ME; Nassiri, M; Arana, M; Perez, MM; Fresno, M; Nadji, M; Vincek, V
      Mapping of genetic deletions on the long arm of chromosome 22 in human pancreatic adenocarcinomas

      ANTICANCER RESEARCH
    30. Tsukamoto, K; Orimo, H; Hosoi, T; Miyao, M; Ota, N; Nakajima, T; Yoshida, H; Watanabe, S; Suzuki, T; Emi, M
      Association of bone mineral density with polymorphism of the human calcium-sensing receptor locus

      CALCIFIED TISSUE INTERNATIONAL
    31. Manuck, SB; Flory, JD; Ferrell, RE; Mann, JJ; Muldoon, MF
      A regulatory polymorphism of the monoamine oxidase-A gene may be associated with variability in aggression, impulsivity, and central nervous system serotonergic responsivity

      PSYCHIATRY RESEARCH
    32. Muneyuki, T; Watanabe, M; Yamanaka, M; Isaji, S; Kawarada, Y; Yatani, R
      Combination analysis of genetic alterations and cell proliferation in small intestinal carcinomas

      DIGESTIVE DISEASES AND SCIENCES
    33. Martin, ER; Menold, MM; Wolpert, CM; Bass, MP; Donnelly, SL; Ravan, SA; Zimmerman, A; Gilbert, JR; Vance, JM; Maddox, LO; Wright, HH; Abramson, RK; DeLong, GR; Cuccaro, ML; Pericak-Vance, MA
      Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    34. Blair, EM; Walsh, S; Oldridge, M; Wall, SS; Wilkie, AOM
      Newly recognised craniosynostosis syndrome that does not map to known disease loci

      AMERICAN JOURNAL OF MEDICAL GENETICS
    35. Weiderpass, E; Persson, I; Melhus, H; Wedren, S; Kindmark, A; Baron, JA
      Estrogen receptor alpha gene polymorphisms and endometrial cancer risk

      CARCINOGENESIS
    36. McDonnell, GV; Kirk, CW; Hawkins, SA; Graham, CA
      An evaluation of interleukin genes fails to identify clear susceptibility loci for multiple sclerosis

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    37. Kunugi, H
      Candidate gene approaches to schizophrenia - Focus on the dopamine hypothesis

      INTERNATIONAL JOURNAL OF MENTAL HEALTH
    38. Curran, B; Lenehan, K; Mulcahy, H; Tighe, O; Bennett, MA; Kay, EW; O'Donoghue, DP; Leader, M; Croke, DT
      Replication error phenotype, clinicopathological variables, and patient outcome in Dukes' B stage II (T3,N0,M0) colorectal cancer

      GUT
    39. Takagi, S; Kinouchi, Y; Hiwatashi, N; Nagashima, F; Chida, M; Takahashi, S; Negoro, K; Shimosegawa, T; Toyota, T
      Relationship between microsatellite instability and telomere shortening incolorectal cancer

      DISEASES OF THE COLON & RECTUM
    40. Comings, DE; Gade-Andavolu, R; Gonzalez, N; Wu, SJ; Muhleman, D; Blake, H; Chiu, F; Wang, E; Farwell, K; Darakjy, S; Baker, R; Dietz, G; Saucier, G; MacMurray, P
      Multivariate analysis of associations of 42 genes in ADHD, ODD and conductdisorder

      CLINICAL GENETICS
    41. Sedivy, R; Wolf, B; Kalipciyan, M; Steger, GG; Karner-Hanusch, J; Mader, RM
      Genetic analysis of multiple synchronous lesions of the colon adenoma-carcinoma sequence

      BRITISH JOURNAL OF CANCER
    42. Ogawa, S; Hosoi, T; Shiraki, M; Orimo, H; Emi, M; Muramatsu, M; Ouchi, Y; Inoue, S
      Association of estrogen receptor beta gene polymorphism with bone mineral density

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    43. Foissac, A; Salhi, M; Cambon-Thomsen, A
      Microsatellites in the HLA region: 1999 update

      TISSUE ANTIGENS
    44. Aguiari, G; Martinello, R; Casaro, D; Rossi, S; Piva, R; Mollica, G; Cavazzini, P; del Senno, L
      LOH of chromosome 6q compared with LOH of 17q and 18q in ovarian cancers: relationship to p53 expression and clinicopathological findings

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
    45. Yaqoob, P; Newsholme, EA; Calder, PC
      Comparison of cytokine production in cultures of whole human blood and purified mononuclear cells

      CYTOKINE
    46. Guilbot, A; Ravise, N; Bouhouche, A; Coullin, P; Birouk, N; Maisonobe, T; Kuntzer, T; Vial, C; Grid, D; Brice, A; LeGuern, E
      Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1

      EUROPEAN JOURNAL OF HUMAN GENETICS
    47. Moncla, A; Malzac, P; Voelckel, MA; Auquier, P; Girardot, L; Mattei, MG; Philip, N; Mattei, JF; Lalande, M; Livet, MO
      Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelmansyndrome patients

      EUROPEAN JOURNAL OF HUMAN GENETICS
    48. Coltman, DW; Bancroft, DR; Robertson, A; Smith, JA; Clutton-Brock, TH; Pemberton, JM
      Male reproductive success in a promiscuous mammal: behavioural estimates compared with genetic paternity

      MOLECULAR ECOLOGY
    49. Flagstad, Q; Roed, K; Stacy, JE; Jakobsen, KS
      Reliable noninvasive genotyping based on excremental PCR of nuclear DNA purified with a magnetic bead protocol

      MOLECULAR ECOLOGY
    50. Bidwell, JL; Wood, NAP; Morse, HR; Olomolaiye, OO; Keen, LJ; Laundy, GJ
      Human cytokine gene nucleotide sequence alignments: supplement 1

      EUROPEAN JOURNAL OF IMMUNOGENETICS
    51. Tarter, R; Vanyukov, M; Giancola, P; Dawes, M; Blackson, T; Mezzich, A; Clark, DB
      Etiology of early age onset substance use disorder: A maturational perspective

      DEVELOPMENT AND PSYCHOPATHOLOGY
    52. Parsian, A
      Sequence analysis of exon 8 of MAO-A gene in alcoholics with antisocial personality and normal controls

      GENOMICS
    53. Bader, P; Klingebiel, T; Schaudt, A; Theurer-Mainka, U; Handgretinger, R; Lang, P; Niethammer, D; Beck, JF
      Prevention of relapse in pediatric patients with acute leukemias and MDS after allogeneic SCT by early immunotherapy initiated on the basis of increasing mixed chimerism: a single center experience of 12 children

      LEUKEMIA
    54. Balasingham, TG; Robinson, NA; McGregor, BA
      Implications for the conservation of genetic diversity in mohair goats from a comparison of a relic island population with breeds farmed in Australia

      AUSTRALIAN JOURNAL OF EXPERIMENTAL AGRICULTURE
    55. Ota, N; Hunt, SC; Nakajima, T; Suzuki, T; Hosoi, T; Orimo, H; Shirai, Y; Emi, M
      Linkage of interleukin 6 locus to human osteopenia by sibling pair analysis

      HUMAN GENETICS
    56. Rybicki, BA; Maliarik, MJ; Malvitz, E; Sheffer, RG; Major, M; Popovich, J; Iannuzzi, MC
      The influence of T cell receptor and cytokine genes on sarcoidosis susceptibility in African Americans

      HUMAN IMMUNOLOGY
    57. Kondo, Y; Kanai, Y; Sakamoto, M; Mizokami, M; Ueda, R; Hirohashi, S
      Microsatellite instability associated with hepatocarcinogenesis

      JOURNAL OF HEPATOLOGY
    58. Curtis, L; Blouin, JL; Radhakrishna, U; Gehrig, C; Lasseter, VK; Wolyniec, P; Nestadt, G; Dombroski, B; Kazazian, HH; Pulver, AE; Housman, D; Bertrand, D; Antonarakis, SE
      No evidence for linkage between schizophrenia and markers at chromosome 15q13-14

      AMERICAN JOURNAL OF MEDICAL GENETICS
    59. Sakamoto, T; Danzmann, RG; Okamoto, N; Ferguson, MM; Ihssen, PE
      Linkage analysis of quantitative trait loci associated with spawning time in rainbow trout (Oncorhynchus mykiss)

      AQUACULTURE
    60. Carreno, H; Paredes, M; Tellez, G; Palomino, H; Blanco, R
      Association between non syndromic cleft lip palate and microsatellite markers located in 6p

      REVISTA MEDICA DE CHILE
    61. Deichmann, KA; Starke, B; Schlenther, S; Heinzmann, A; Sparholt, SH; Forster, J; Kuehr, J
      Linkage and association studies of atopy and the chromosome 11q13 region

      JOURNAL OF MEDICAL GENETICS
    62. Thornton, MA; Poncz, M; Korostishevsky, M; Yakobson, E; Usher, S; Seligsohn, U; Peretz, H
      The human platelet alpha IIb gene is not closely linked to its integrin partner beta 3

      BLOOD
    63. Kunnas, TA; Holmberg-Marttila, D; Karhunen, PJ
      Analysis of estrogen receptor dinucleotide polymorphism by capillary gel electrophoresis with a population genetic study in 180 Finns

      HUMAN HEREDITY
    64. WATANABE I; TSUKAMOTO K; SHIBA T; EMI M
      ISOLATION AND RADIATION HYBRID MAPPING OF DINUCLEOTIDE REPEAT POLYMORPHISM AT THE HUMAN MATRIX GLA PROTEIN (MGP) LOCUS

      JOURNAL OF HUMAN GENETICS
    65. Palmer, LJ; Daniels, SE; Rye, PJ; Gibson, NA; Tay, GK; Cookson, WOCM; Goldblatt, J; Burton, PR; LeSouef, PN
      Linkage of chromosome 5q and 11q gene markers to asthma-associated quantitative traits in Australian children

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    66. CHRISTIAN SL; BHATT NK; MARTIN SZ; SUTCLIFFE JS; KUBOTA T; HUANG B; MUTIRANGURA A; CHINAULT AC; BEAUDET AL; LEDBETTER DH
      INTEGRATED YAC CONTIG MAP OF THE PRADER-WILLI ANGELMAN-REGION ON CHROMOSOME-15Q11-Q13 WITH AVERAGE STS SPACING OF 35-KB/

      PCR methods and applications
    67. JOHN S; KORMAN Y; OLLIER W; WORTHINGTON J
      INTEGRATED MICROSATELLITE MARKERS SUITABLE FOR GENETIC-STUDIES OF CYTOKINE GENES

      Cytokine (Philadelphia, Pa. Print)
    68. Li, PN; Thompson, JN; Wang, XY; Song, L
      Analysis of common mutations and associated haplotypes in Chinese patientswith glucose-6-phosphate dehydrogenase deficiency

      BIOCHEMISTRY AND MOLECULAR BIOLOGY INTERNATIONAL
    69. BUGGE M; COLLINS A; PETERSEN MB; FISHER J; BRANDT C; HERTZ JM; TRANEBJAERG L; DELOZIERBLANCHET C; NICOLAIDES P; BRONDUMNIELSEN K; MORTON N; MIKKELSEN M
      NONDISJUNCTION OF CHROMOSOME-18

      Human molecular genetics
    70. MARSHALL TC; SLATE J; KRUUK LEB; PEMBERTON JM
      STATISTICAL CONFIDENCE FOR LIKELIHOOD-BASED PATERNITY INFERENCE IN NATURAL-POPULATIONS

      Molecular ecology
    71. KONISHI H; TAKAHASHI T; KOZAKI K; YATABE Y; MITSUDOMI T; FUJII Y; SUGIURA T; MATSUDA H; TAKAHASHI T; TAKAHASHI T
      DETAILED DELETION MAPPING SUGGESTS THE INVOLVEMENT OF A TUMOR-SUPPRESSOR GENE AT 17P13.3, DISTAL TO P53, IN THE PATHOGENESIS OF LUNG CANCERS

      Oncogene
    72. CHEN QY; LAN MS; SHE JX; MACLAREN NK
      THE GENE RESPONSIBLE FOR AUTOIMMUNE POLYGLANDULAR SYNDROME TYPE-1 MAPS TO CHROMOSOME 21Q22.3 IN US PATIENTS

      Journal of autoimmunity
    73. MORGAN RJ; NEWCOMB PV; BAILEY M; HARDWICK RH; ALDERSON D
      LOSS OF HETEROZYGOSITY AT MICROSATELLITE MARKER SITES FOR TUMOR-SUPPRESSOR GENES IN ESOPHAGEAL ADENOCARCINOMA

      European journal of surgical oncology
    74. ESTOUP A; GHARBI K; SANCRISTOBAL M; CHEVALET C; HAFFRAY P; GUYOMARD R
      PARENTAGE ASSIGNMENT USING MICROSATELLITES IN TURBOT (SCOPHTHALMUS-MAXIMUS) AND RAINBOW-TROUT (ONCORHYNCHUS-MYKISS) HATCHERY POPULATIONS

      Canadian journal of fisheries and aquatic sciences
    75. SAITOH H; UEDA S; KUROSAKI K; KIUCHI M
      THE DIFFERENT MOBILITY OF COMPLEMENTARY STRANDS DEPENDS ON THE PROPORTION AC GT/

      Forensic science international
    76. SABOL SZ; HU S; HAMER D
      A FUNCTIONAL POLYMORPHISM IN THE MONOAMINE-OXIDASE-A GENE PROMOTER

      Human genetics
    77. WALTZ MR; PANDELIDIS SM; PRATT W; BARNES D; SWALLOW DM; GENDLER SJ; COHEN EP
      A MICROSATELLITE WITHIN THE MUC1 LOCUS AT 1Q21 IS ALTERED IN THE NEOPLASTIC-CELLS OF BREAST-CANCER PATIENTS

      Cancer genetics and cytogenetics
    78. NAKAMOTO JM; SANDSTROM AT; BRICKMAN AS; CHRISTENSON RA; VANDOP C
      PSEUDOHYPOPARATHYROIDISM TYPE IA FROM MATERNAL BUT NOT PATERNAL TRANSMISSION OF A G(S)ALPHA GENE MUTATION

      American journal of medical genetics
    79. SAITO K; KONDOIIDA E; KAWAKITA Y; JUAN D; IKEYA K; OSAWA M; FUKUYAMA Y; TODA T; NAKABAYASHI M; YAMAMOTO T; KOBAYASHI M
      PRENATAL-DIAGNOSIS OF FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY IN 8 JAPANESE FAMILIES BY HAPLOTYPE ANALYSIS USING NEW MARKERS CLOSEST TOTHE GENE

      American journal of medical genetics
    80. SHINMURA K; TANI M; ISOGAKI J; WANG Y; SUGIMURA H; YOKOTA J
      RER PHENOTYPE AND ITS ASSOCIATED MUTATIONS IN FAMILIAL GASTRIC-CANCER

      Carcinogenesis
    81. MERTENS C; BRASSAT D; REBOUL J; EICHENBAUMVOLINE S; VUILLEMINAZAIS C; COURNU I; BABRON MC; SEMANA G; EDAN G; CLANET M; CLERGETDARPOUX F; EVERCOOREN ABV; LYONCAEN O; LIBLAU R; FONTAINE B
      A SYSTEMATIC STUDY OF OLIGODENDROCYTE GROWTH-FACTORS AS CANDIDATES FOR GENETIC SUSCEPTIBILITY TO MS

      Neurology
    82. PATERSON S; WILSON K; PEMBERTON JM
      MAJOR HISTOCOMPATIBILITY COMPLEX VARIATION ASSOCIATED WITH JUVENILE SURVIVAL AND PARASITE RESISTANCE IN A LARGE UNMANAGED UNGULATE POPULATION (OVIS-ARIES L.)

      Proceedings of the National Academy of Sciences of the United Statesof America
    83. ESPINOS C; NAJERA C; MILLAN JM; AYUSO C; BAIGET M; PEREZGARRIGUES H; RODRIGO O; VILELA C; BENEYTO M
      LINKAGE ANALYSIS IN USHER-SYNDROME TYPE-I (USH1) FAMILIES FROM SPAIN

      Journal of Medical Genetics
    84. ROBINSON R; CURRAN JL; HALL WJ; HALSALL PJ; HOPKINS PM; MARKHAM AF; STEWART AD; WEST SP; ELLIS FR
      GENETIC-HETEROGENEITY AND HOMOG ANALYSIS IN BRITISH MALIGNANT HYPERTHERMIA FAMILIES

      Journal of Medical Genetics
    85. PATERSON S
      EVIDENCE FOR BALANCING SELECTION AT THE MAJOR HISTOCOMPATIBILITY COMPLEX IN A FREE-LIVING RUMINANT

      Journal of heredity
    86. JACKSON TR; FERGUSON MM; DANZMANN RG; FISHBACK AG; IHSSEN PE; OCONNELL M; CREASE TJ
      IDENTIFICATION OF 2 QTL INFLUENCING UPPER TEMPERATURE TOLERANCE IN 3 RAINBOW-TROUT (ONCORHYNCHUS-MYKISS) HALF-SIB FAMILIES

      Heredity
    87. Roed, KH
      Microsatellite variation in Scandinavian Cervidae using primers derived from Bovidae

      HEREDITAS
    88. LOUHELAINEN J; LINDSTROM E; HEMMINKI K; TOFTGARD R
      DINUCLEOTIDE REPEAT POLYMORPHISM WITHIN THE TUMOR-SUPPRESSOR GENE PTCH AT 9Q22

      Clinical genetics
    89. MINAGUCHI T; KANAMORI Y; MATSUSHIMA M; YOSHIKAWA H; TAKETANI Y; NAKAMURA Y
      NO EVIDENCE OF CORRELATION BETWEEN POLYMORPHISM AT CODON-72 OF P53 AND RISK OF CERVICAL-CANCER IN JAPANESE PATIENTS WITH HUMAN-PAPILLOMAVIRUS-16 HUMAN-PAPILLOMAVIRUS-18 INFECTION/

      Cancer research
    90. CHIANG JM; CHOU YHW; CHOU TB
      K-RAS CODON-12 MUTATION DETERMINES THE POLYPOID GROWTH OF COLORECTAL-CANCER

      Cancer research
    91. OKLADNOVA O; SYAGAILO YV; TRANITZ M; STOBER G; RIEDERER P; MOSSNER R; LESCH KP
      A PROMOTER-ASSOCIATED POLYMORPHIC REPEAT MODULATES PAX-6 EXPRESSION IN HUMAN BRAIN

      Biochemical and biophysical research communications (Print)
    92. TAN FK; STIVERS DN; FOSTER MW; CHAKRABORTY R; HOWARD RF; MILEWICZ DM; ARNETT FC
      ASSOCIATION OF MICROSATELLITE MARKERS NEAR THE FIBRILLIN-1 GENE ON HUMAN-CHROMOSOME 15Q WITH SCLERODERMA IN A NATIVE-AMERICAN POPULATION

      Arthritis and rheumatism
    93. JOHN S; MYERSCOUGH A; MARLOW A; HAJEER A; SILMAN A; OLLIER W; WORTHINGTON J
      LINKAGE OF CYTOKINE GENES TO RHEUMATOID-ARTHRITIS - EVIDENCE OF GENETIC-HETEROGENEITY

      Annals of the Rheumatic Diseases
    94. FIELD LL; KAPLAN BJ
      ABSENCE OF LINKAGE OF PHONOLOGICAL CODING DYSLEXIA TO CHROMOSOME 6P23-P21.3 IN A LARGE FAMILY DATA SET

      American journal of human genetics
    95. BUITING K; DITTRICH B; GROSS S; LICH C; FARBER C; BUCHHOLZ T; SMITH E; REIS A; BURGER J; NOTHEN MM; BARTHWITTE U; JANSSEN B; ABELIOVICH D; LERER I; VANDENOUWELAND AMW; HALLEY DJJ; SCHRANDERSTUMPEL C; SMEETS H; MEINECKE P; MALCOLM S; GARDNER A; LALANDE M; NICHOLLS RD; FRIEND K; SCHULZE A; MATTHIJS G; KOKKONEN H; HILBERT P; VANMALDERGEM L; GLOVER G; CARBONELL P; WILLEMS P; GILLESSENKAESBACH G; HORSTHEMKE B
      SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS

      American journal of human genetics
    96. MENOLD MM; SADEH M; LENNON F; BLATT I; GOLDHAMMER Y; YAMAOKA LH; VANCE JM; PERICAKVANCE MA
      EVIDENCE FOR GENETIC-HETEROGENEITY SUPPORTS CLINICAL DIFFERENCES IN CONGENITAL MYASTHENIC SYNDROMES

      Human heredity
    97. FOISSAC A; CAMBONTHOMSEN A
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      Tissue antigens
    98. STRATAKIS CA; SARLIS NJ; BERRETTINI WH; BADNER JA; CHROUSOS GP; GERSHON ES; DETERAWADLEIGH SD
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      Molecular psychiatry
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      NCAM AND SCHIZOPHRENIA - GENETIC-STUDIES

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 06:48:11