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    1. Ikari, K; Onda, H; Furushima, K; Maeda, S; Harata, S; Takeda, J
      Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population

      JOURNAL OF HUMAN GENETICS
    2. Romney, CA; Paulauskis, JD; Little, JB
      X-ray induction of microsatellite instability at autosomal loci in human lymphoblastoid WTK1 cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    3. Soares, RPS; Chamone, DAF; Bydlowski, SP
      Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis

      HAEMOPHILIA
    4. Meekins, JF; Ballard, HE; McCarthy, BC
      Genetic variation and molecular biogeography of a North American invasive plant species (Alliaria petiolata, Brassicaceae)

      INTERNATIONAL JOURNAL OF PLANT SCIENCES
    5. Lebo, RV; Maher, T; Farrer, L; Fenerci, EY; Milunsky, JM
      Highly polymorphic short tandem repeat analyses clarify complex molecular test results

      DIAGNOSTIC MOLECULAR PATHOLOGY
    6. Alonso, J; Garcia-Miguel, P; Abelairas, J; Mendiola, M; Pestana, A
      A microsatellite fluorescent method for linkage analysis in familial retinoblastoma and deletion detection at the RBI locus in retinoblastoma and osteosarcoma

      DIAGNOSTIC MOLECULAR PATHOLOGY
    7. Bauer, A; Savelyeva, L; Claas, A; Praml, C; Berthold, F; Schwab, M
      Smallest region of overlapping deletion in I p36 in human neuroblastoma: AI Mbp cosmid and PAC contig

      GENES CHROMOSOMES & CANCER
    8. Sardi, I; Franchi, A; Bocciolini, C; Mechi, C; Frittelli, A; Bruschini, L; Gallo, O
      Microsatellite instability as biomarker for risk of multiple primary malignancies of the upper aerodigestive tract

      ONCOLOGY REPORTS
    9. Serra, E; Ars, E; Ravella, A; Sanchez, A; Puig, S; Rosenbaum, T; Estivill, X; Lazaro, C
      Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations

      HUMAN GENETICS
    10. Li, A; Ge, S
      Genetic variation and clonal diversity of Psammochloa villosa (Poaceae) detected by ISSR markers

      ANNALS OF BOTANY
    11. Casasoli, M; Mattioni, C; Cherubini, M; Villani, F
      A genetic linkage map of European chestnut (Castanea sativa Mill.) based on RAPD, ISSR and isozyme markers

      THEORETICAL AND APPLIED GENETICS
    12. Mesa, MS; Arroyo-Pardo, E; Martinez-Labarga, C; Ocana, MA; Arroyo, M; Bandres, F
      Variability of six STR loci in populations from Central Spain

      HUMAN BIOLOGY
    13. Lai, JA; Yang, WC; Hsiao, JY
      An assessment of genetic relationships in cultivated tea clones and nativewild tea in Taiwan using RAPD and ISSR maskers

      BOTANICAL BULLETIN OF ACADEMIA SINICA
    14. Meschede, D; Dworniczak, B; Behre, HM; Nieschlag, E; Horst, J
      No evidence for uniparental disomy of the sex chromosomes in idiopathic male infertility

      MOLECULAR HUMAN REPRODUCTION
    15. Yoshida, T; Sugai, T; Habano, W; Nakamura, S; Uesugi, N; Funato, O; Saito, K
      Microsatellite instability in gallbladder carcinoma: two independent genetic pathways of gallbladder carcinogenesis

      JOURNAL OF GASTROENTEROLOGY
    16. Leroy, XJ; Leon, K; Charles, G; Branchard, M
      Cauliflower somatic embryogenesis and analysis of regenerant stability by ISSRs

      PLANT CELL REPORTS
    17. Perez, T; Albornoz, J; Dominguez, A
      A panel of bovine and caprine microsatellites suitable as markers in chamois

      ANIMAL GENETICS
    18. Maddox, JF
      Chromosomal assignments and polymorphism information content in sheep for 12 cattle microsatellites

      ANIMAL GENETICS
    19. Maddox, JF; Schibler, L; Cribiu, EP; Kang, N; Davies, KP; Vaiman, D
      Linkage mapping of goat ChirUCO, LSCV and SR-CRSP microsatellites in sheep

      ANIMAL GENETICS
    20. Arcade, A; Anselin, F; Rampant, PF; Lesage, MC; Paques, LE; Prat, D
      Application of AFLP, RAPD and ISSR markers to genetic mapping of European and Japanese larch

      THEORETICAL AND APPLIED GENETICS
    21. John, AM; Ruggieri, M; Ferner, R; Upadhyaya, M
      A search for evidence of somatic mutations in the NF1 gene

      JOURNAL OF MEDICAL GENETICS
    22. Allayee, H; Dominguez, KM; Aouizerat, BE; Krauss, RM; Rotter, JI; Lu, JY; Cantor, RM; de Bruin, TWA; Lusis, AJ
      Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia

      JOURNAL OF LIPID RESEARCH
    23. Ingvarsson, S; Finnsdottir, V; Sigurdsson, A; Geirsson, G
      Population studies and validation of paternity determinations by six microsatellite loci

      JOURNAL OF FORENSIC SCIENCES
    24. Schneider, BG; Bravo, JC; Roa, JC; Roa, I; Kim, MC; Lee, KM; Plaisance, KT; McBride, CM; Mera, R
      Microsatellite instability, prognosis and metastasis in gastric cancers from a low-risk population

      INTERNATIONAL JOURNAL OF CANCER
    25. Eisenbarth, I; Beyer, K; Krone, W; Assum, G
      Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. Antonius-Klemola, K
      Molecular markers in Rubus (Rosaceae) research and breeding

      JOURNAL OF HORTICULTURAL SCIENCE & BIOTECHNOLOGY
    27. EL-Maarri, O; Kavakli, K; Caglayan, SH
      Intron 22 inversions in the Turkish haemophilia A patients: prevalence andhaplotype analysis

      HAEMOPHILIA
    28. Elgadi, KM; Meguid, RA; Qian, M; Souba, WW; Abcouwer, SF
      Cloning and analysis of unique human glutaminase isoforms generated by tissue-specific alternative splicing

      PHYSIOLOGICAL GENOMICS
    29. Sardi, I; Bartoletti, R; Occhini, I; Piazzini, M; Travaglini, F; Guazzelli, R; Montali, E
      Microsatellite alterations in superficial and locally advanced transitional cell carcinoma of the bladder

      ONCOLOGY REPORTS
    30. Guo, C; White, PS; Weiss, MJ; Hogarty, MD; Thompson, PM; Stram, DO; Gerbing, R; Matthay, KK; Seeger, RC; Brodeur, GM; Maris, JM
      Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas

      ONCOGENE
    31. Pineau, P; Nagai, H; Prigent, S; Wei, Y; Gyapay, G; Weissenbach, J; Tiollais, P; Buendia, MA; Dejean, A
      Identification of three distinct regions of allelic deletions on the shortarm of chromosome 8 in hepatocellular carcinoma

      ONCOGENE
    32. Henke, L; Fimmers, R; Josephi, E; Cleef, S; Dulmer, M; Henke, J
      Usefulness of conventional blood groups, DNA-minisatellites, and short tandem repeat polymorphisms in paternity testing: a comparison

      FORENSIC SCIENCE INTERNATIONAL
    33. Cozzi, J; Conn, CM; Harper, J; Winston, RML; Rindl, M; Farndon, PA; Delhanty, JDA
      A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception

      HUMAN GENETICS
    34. Pfeiffer, RA; Rauch, A; Trautmann, U; Dorr, HG; Hiort, O; Scherer, G; Rosch, G; Papadopoulos, T; Van der Hardt, K; Lachmann, E
      Defective sexual development in an infant with 46, XY, der(9)t(8;9)(q23.1;p23)mat

      EUROPEAN JOURNAL OF PEDIATRICS
    35. Luft, F; Gebert, J; Schneider, A; Melsheimer, P; Doeberitz, MV
      Frequent allelic imbalance of tumor suppressor gene loci in cervical dysplasia

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    36. Luikart, G; Biju-Duval, MP; Ertugrul, O; Zagdsuren, Y; Maudet, C; Taberlet, P
      Power of 22 microsatellite markers in fluorescent multiplexes for parentage testing in goats (Capra hircus)

      ANIMAL GENETICS
    37. van Hooft, WF; Hanotte, O; Wenink, PW; Groen, AF; Sugimoto, Y; Prins, HHT; Teale, A
      Applicability of bovine microsatellite markers for population genetic studies on African buffalo (Syncerus caffer)

      ANIMAL GENETICS
    38. Ashton-Prolla, P; Ashley, GA; Giugliani, R; Pires, RF; Desnick, RJ; Eng, CM
      Fabry disease: Comparison of enzymatic, linkage, and mutation analysis forcarrier detection in a family with a novel mutation (30delG)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    39. Miyahci, H; Ma, L; Takemura, Y; Kobayashi, H; Hirahara, I; Sonehara, H; Ando, Y
      Microsatellite instability and clonal heterogeneity of MDR1 messenger RNA expression ln trimetrexate-resistant human leukemia MOLT-3 cells developed in thymidine

      INTERNATIONAL JOURNAL OF CANCER
    40. Joshi, SP; Ranjekar, PK; Gupta, VS
      Molecular markers in plant genome analysis

      CURRENT SCIENCE
    41. Liu, XD; Barker, DF
      Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1

      AMERICAN JOURNAL OF HUMAN GENETICS
    42. CALAFELL F; SHUSTER A; SPEED WC; KIDD JR; KIDD KK
      SHORT TANDEM REPEAT POLYMORPHISM EVOLUTION IN HUMANS

      European journal of human genetics
    43. STONE DL; AGARWALA R; SCHAFFER AA; WEBER JL; VASKE D; ODA T; CHANDRASEKHARAPPA SC; FRANCOMANO CA; BIESECKER LG
      GENETIC AND PHYSICAL MAPPING OF THE MCKUSICK-KAUFMAN-SYNDROME

      Human molecular genetics
    44. MACDONALD GA; GREENSON JK; SAITO K; CHERIAN SP; APPELMAN HD; BOLAND CR
      MICROSATELLITE INSTABILITY AND LOSS OF HETEROZYGOSITY AT DNA MISMATCHREPAIR GENE LOCI OCCURS DURING HEPATIC CARCINOGENESIS

      Hepatology
    45. SLATE J; COLTMAN DW; GOODMAN SJ; MACLEAN I; PEMBERTON JM; WILLIAMS JL
      BOVINE MICROSATELLITE LOCI ARE HIGHLY CONSERVED IN RED DEER (CERVUS-ELAPHUS), SIKA-DEER (CERVUS-NIPPON) AND SOAY SHEEP (OVIS-ARIES)

      Animal genetics
    46. SIRCHIA SM; GARAGIOLA I; COLUCCI G; GUERNERI S; LALATTA F; GRIMOLDI MG; SIMONI G
      TRISOMIC ZYGOTE RESCUE REVEALED BY DNA POLYMORPHISM ANALYSIS IN CONFINED PLACENTAL MOSAICISM

      Prenatal diagnosis
    47. MISCICKASLIWKA D; GRZYBOWSKI T; CZARNY J; WOZNIAK M
      SCREENING OF A HIGHLY POLYMORPHIC MICROSATELLITE FOR MICROHETEROGENEITY IN HUMAN IDENTIFICATION

      Electrophoresis
    48. Oetting, WS; Armstrong, CM; Ronan, SM; Young, TL; Sellers, TA; King, RA
      Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detection

      ELECTROPHORESIS
    49. TALWALKAR VR; SCHEINER M; HEDGES LK; BUTLER MG; SCHWARTZ HS
      MICROSATELLITE INSTABILITY IN MALIGNANT-MELANOMA

      Cancer genetics and cytogenetics
    50. WHITE VA; MCNEIL BK; HORSMAN DE
      ACQUIRED HOMOZYGOSITY (ISODISOMY) OF CHROMOSOME-3 IN UVEAL MELANOMA

      Cancer genetics and cytogenetics
    51. Soyke, A; Stumm, M; Krebs, P; Kloos, DU; Wieacker, P; Elsner, J; Mohnike, K
      Familial occurrence of a del(Xp-) chromosome: Pitfall in karyotype/phenotype correlation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. KANTHASWAMY S; SMITH DG
      USE OF MICROSATELLITE POLYMORPHISMS FOR PATERNITY EXCLUSION IN RHESUSMACAQUES (MACACA-MULATTA)

      Primates
    53. THORNTON PS; SATINSMITH MS; HEROLD K; GLASER B; CHIU KC; NESTOROWICZ A; PERMUTT MA; BAKER L; STANLEY CA
      FAMILIAL HYPERINSULINISM WITH APPARENT AUTOSOMAL-DOMINANT INHERITANCE- CLINICAL AND GENETIC-DIFFERENCES FROM THE AUTOSOMAL RECESSIVE VARIANT

      The Journal of pediatrics
    54. MASTAGLIA FL; HARKER N; PHILLIPS BA; DAY TJ; HANKEY GJ; LAING NG; FABIAN V; KAKULAS BA
      DOMINANTLY INHERITED PROXIMAL MYOTONIC MYOPATHY AND LEUKOENCEPHALOPATHY IN A FAMILY WITH AN INCIDENTAL CLCN1 MUTATION

      Journal of Neurology, Neurosurgery and Psychiatry
    55. RASMUSSEN SA; COLMAN SD; HO VT; ABERNATHY CR; ARN PH; WEISS L; SCHWARTZ C; SAUL RA; WALLACE MR
      CONSTITUTIONAL AND MOSAIC LARGE NF1 GENE DELETIONS IN NEUROFIBROMATOSIS TYPE-1

      Journal of Medical Genetics
    56. WEBB T; CLARKE A; HANEFELD F; PEREIRA JL; ROSENBLOOM L; WOODS CG
      LINKAGE ANALYSIS IN RETT-SYNDROME FAMILIES SUGGESTS THAT THERE MAY BEA CRITICAL REGION AT XQ28

      Journal of Medical Genetics
    57. ESPOSITO DL; PALMIROTTA R; VERI MC; MAMMARELLA S; DAMICO F; CURIA MC; ACETO G; CROGNALE S; CREATI B; MARIANICOSTANTINI R; BATTISTA P; CAMA A
      OPTIMIZED PCR LABELING IN MUTATIONAL AND MICROSATELLITE ANALYSIS

      Clinical chemistry
    58. LEE MJ; NISHIO H; NAGAI T; OKAMOTO N; YUKI T; SUMINO K
      MOLECULAR-GENETIC ANALYSIS OF THE PRADER-WILLI-SYNDROME BY USING FLUORESCENT MULTIPLEX PCR OF THE DINUCLEOTIDE REPEATS ON CHROMOSOME 15Q11-Q13

      Clinica chimica acta
    59. TANOSAKI S; INOKUCHI K; SHIMADA T; DAN K
      RELATION BETWEEN MICROSATELLITE INSTABILITY AND N-RAS MUTATION AND DURATION OF DISEASE-FREE SURVIVAL IN PATIENTS WITH ACUTE-LEUKEMIA

      Cancer
    60. YOUNG TL; RONAN SM; DRAHOZAL LA; WILDENBERG SC; ALVEAR AB; OETTING WS; ATWOOD LD; WILKIN DJ; KING RA
      EVIDENCE THAT A LOCUS FOR FAMILIAL HIGH MYOPIA MAPS TO CHROMOSOME 18P

      American journal of human genetics
    61. PAJUKANTA P; PORKKA KVK; ANTIKAINEN M; TASKINEN MR; PEROLA M; MURTOMAKIREPO S; EHNHOLM S; NUOTIO I; SUURINKEROINEN L; LAHDENKARI AT; SYVANEN AC; VIIKARI JSA; EHNHOLM C; PELTONEN L
      NO EVIDENCE OF LINKAGE BETWEEN FAMILIAL COMBINED HYPERLIPIDEMIA AND GENES ENCODING LIPOLYTIC ENZYMES IN FINNISH FAMILIES

      Arteriosclerosis, thrombosis, and vascular biology
    62. DEMARCHIS L; CONTEGIACOMO A; DAMICO C; PALMIROTTA R; PIZZI C; OTTINI L; MASTRANZO P; FIGLIOLINI M; PETRELLA G; AMANTI C; BATTISTA P; BIANCO AR; FRATI L; CAMA A; MARIANICOSTANTINI R
      MICROSATELLITE INSTABILITY IS CORRELATED WITH LYMPH NODE-POSITIVE BREAST-CANCER

      Clinical cancer research
    63. KAPPES SM; KEELE JW; STONE RT; SONSTEGARD TS; SMITH TPL; MCGRAW RA; LOPEZCORRALES NL; BEATTIE CW
      A 2ND-GENERATION LINKAGE MAP OF THE BOVINE GENOME

      PCR methods and applications
    64. CHOI C; CHO SH; HORIKAWA I; BERCHUCK A; WANG N; CEDRONE E; JHUNG SW; LEE JB; KERR J; CHENEVIXTRENCH G; KIM SY; BARRETT JC; KOI M
      LOSS OF HETEROZYGOSITY AT CHROMOSOME SEGMENT XQ25-26.1 IN ADVANCED HUMAN OVARIAN CARCINOMAS

      Genes, chromosomes & cancer
    65. HALL IJ; GIOELI D; WEISSMAN BE; TISTY TD
      IDENTIFICATION OF ADDITIONAL COMPLEMENTATION GROUPS THAT REGULATE GENOMIC INSTABILITY

      Genes, chromosomes & cancer
    66. KOBAYASHI K; KONDO K; IKEDA I; KANEKO S; SAKAI N; YOSHIDA M; HOSAKA M; NAGASHIMA Y; SHUIN T; YAO M
      MICROSATELLITE INSTABILITY OCCURS INFREQUENTLY IN SPORADIC RENAL-CELLCARCINOMA

      Oncology Reports
    67. BATTISTA P; PALMIROTTA R; VITULLO P; VERI MC; COLALONGO C; RIGOLI L; FEDELE F; CARUSO R; INFERRERA C; ROMANO F; MARIANICOSTANTINI R; FRATI L; CAMA A
      MICROSATELLITE INSTABILITY IN EARLY GASTRIC-CANCER

      International journal of oncology
    68. SULISALO T; MAKITIE O; SISTONEN P; RIDANPAA M; ELRIFAI W; RUUSKANAEN O; DELACHAPELLE A; KAITILA I
      UNIPARENTAL DISOMY IN CARTILAGE-HAIR HYPOPLASIA

      European journal of human genetics
    69. KLOOS DU; JAKUBICZKA S; WIENKER T; WOLFF G; WIEACKER P
      LOCALIZATION OF THE GENE FOR WIEACKER-WOLFF-SYNDROME IN THE PERICENTROMERIC REGION OF THE X-CHROMOSOME

      Human genetics
    70. DEGORTARI MJ; FREKING BA; KAPPES SM; LEYMASTER KA; CRAWFORD AM; STONE RT; BEATTIE CW
      EXTENSIVE GENOMIC CONSERVATION OF CATTLE MICROSATELLITE HETEROZYGOSITY IN SHEEP

      Animal genetics
    71. SIRCHIA SM; PARIANI S; ROSSELLA F; GARAGIOLA I; DEANDREIS C; BULFAMANTE G; ZANNONI E; RADAELLI U; SIMONI G
      CYTOGENETIC ABNORMALITIES AND MICROSATELLITE INSTABILITY IN ENDOMETRIAL ADENOCARCINOMA

      Cancer genetics and cytogenetics
    72. CAGGANA M; ASHLEY GA; DESNICK RJ; ENG CM
      FABRY-DISEASE - MOLECULAR CARRIER DETECTION AND PRENATAL-DIAGNOSIS BYANALYSIS OF CLOSELY LINKED POLYMORPHISMS AT XQ22.1

      American journal of medical genetics
    73. SERRA A; BOVA R; BELLANOVA G; CHINDEMI A; ZAPPATA S; BRAHE C
      PARTIAL 9P MONOSOMY IN A GIRL WITH A TDIC(9P23-13P11) TRANSLOCATION, MINOR ANOMALIES, OBESITY, AND MENTAL-RETARDATION

      American journal of medical genetics
    74. MCGINNISS MJ; BROWN DH; BURKE LW; MASCARELLO JT; JONES MC
      RING CHROMOSOME-X IN A CHILD WITH MANIFESTATIONS OF KABUKI-SYNDROME

      American journal of medical genetics
    75. SULLIVAN KE; VEKSLER E; LEDERMAN H; LEESMILLER SP
      CELL-CYCLE CHECKPOINTS AND DNA-REPAIR IN NIJMEGEN BREAKAGE SYNDROME

      Clinical immunology and immunopathology
    76. OGATA T; MUROYA I; MATSUO N; HATA J; FUKUSHIMA Y; SUZUKI Y
      IMPAIRED MALE SEX DEVELOPMENT IN AN INFANT WITH MOLECULARLY DEFINED PARTIAL 9P MONOSOMY - IMPLICATION FOR A TESTIS FORMING GENE(S) ON 9P

      Journal of Medical Genetics
    77. LURIA D; AVIGAD S; COHEN IJ; STARK B; WEITZ R; ZAIZOV R
      P53 MUTATION AS THE 2ND EVENT IN JUVENILE CHRONIC MYELOGENOUS LEUKEMIA IN A PATIENT WITH NEUROFIBROMATOSIS TYPE-1

      Cancer
    78. EISENBARTH I; ASSUM G; KAUFMANN D; KRONE W
      EVIDENCE FOR THE PRESENCE OF THE 2ND ALLELE OF THE NEUROFIBROMATOSIS TYPE-1 GENE IN MELANOCYTES DERIVED FROM CAFE AU LAIT MACULES OF NF1 PATIENTS

      Biochemical and biophysical research communications
    79. DASCHNER K; ASSUM G; EISENBARTH I; KRONE W; HOFFMEYER S; WORTMANN S; HEYMER B; KEHRERSAWATZKI H
      CLONAL ORIGIN OF TUMOR-CELLS IN A PLEXIFORM NEUROFIBROMA WITH LOH IN NF1 INTRON-38 AND IN DERMAL NEUROFIBROMAS WITHOUT LOH OF THE NF1 GENE

      Biochemical and biophysical research communications
    80. JAMES RS; DALTON P; GUSTASHAW K; WOLFF DJ; WILLARD HF; MITCHELL C; JACOBS PA
      MOLECULAR CHARACTERIZATION OF ISOCHROMOSOMES OF XQ

      Annals of Human Genetics
    81. OHYASHIKI JH; OHYASHIKI K; AIZAWA S; KAWAKUBO K; SHIMAMOTO T; IWAMA H; HAYASHI S; TOYAMA K
      REPLICATION ERRORS IN HEMATOLOGICAL NEOPLASIAS - GENOMIC INSTABILITY IN PROGRESSION OF DISEASE IS DIFFERENT AMONG DIFFERENT TYPES OF LEUKEMIA

      Clinical cancer research
    82. CORLESS CL; ABURATANI H; FLETCHER JA; HOUSMAN DE; AMIN MB; WEINBERG DS
      PAPILLARY RENAL-CELL CARCINOMA - QUANTITATION OF CHROMOSOME-7 AND CHROMOSOME-17 BY FISH, ANALYSIS OF CHROMOSOME 3P FOR LOH, AND DNA-PLOIDY

      Diagnostic molecular pathology
    83. TOMKINS DJ; ROUX AF; WAYE J; FREEMAN VCP; COX DW; WHELAN DT
      MATERNAL UNIPARENTAL ISODISOMY OF HUMAN-CHROMOSOME-14 ASSOCIATED WITHA PATERNAL T(13Q14Q) AND PRECOCIOUS PUBERTY

      European journal of human genetics
    84. KAYSER M; RITTER H; BERCOVITCH F; MRUG M; ROEWER L; NURNBERG P
      IDENTIFICATION OF HIGHLY POLYMORPHIC MICROSATELLITES IN THE RHESUS MACAQUE MACACA-MULATTA BY CROSS-SPECIES AMPLIFICATION

      Molecular ecology
    85. JASS JR; POKOS V; ARNOLD JL; COTTIER DS; JEEVARATNAM P; VANDEWATER NS; BROWETT PJ; WINSHIP IM; LANE MR
      COLORECTAL NEOPLASMS DETECTED COLONOSCOPICALLY IN AT-RISK MEMBERS OF COLORECTAL-CANCER FAMILIES STRATIFIED BY THE DEMONSTRATION OF DNA MICROSATELLITE INSTABILITY

      Journal of molecular medicine
    86. SIRCHIA SM; GARAGIOLA I; DEANDREIS C; GAZZOLI I; GRAMEGNA M; COLUCCI G
      CHARACTERIZATION OF 4 MICROSATELLITES IN AN ITALIAN POPULATION AND THEIR APPLICATION TO PATERNITY TESTING

      Molecular and cellular probes
    87. IMBERT A; CHAFFANET M; ESSIOUX L; NOGUCHI T; ADELAIDE J; KERANGUEVEN F; LEPASLIER D; BONAITIPELLIE C; SOBOL H; BIRNBAUM D; PEBUSQUE MJ
      INTEGRATED MAP OF THE CHROMOSOME 8P12-P21 REGION, A REGION INVOLVED IN HUMAN CANCERS AND WERNER SYNDROME

      Genomics
    88. RIVA P; CASTORINA P; MANOUKIAN S; DALPRA L; DONEDA L; MARINI G; DENDUNNEN J; LARIZZA L
      CHARACTERIZATION OF A CYTOGENETIC 17Q11.2 DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME

      Human genetics
    89. FUQUA JS; SHER ES; PERLMAN EJ; URBAN MD; GHAHREMANI M; PELLETIER J; MIGEON CJ; BROWN TR; BERKOVITZ GD
      ABNORMAL GONADAL DIFFERENTIATION IN 2 SUBJECTS WITH AMBIGUOUS GENITALIA, MULLERIAN STRUCTURES, AND NORMALLY DEVELOPED TESTES - EVIDENCE FORA DEFECT IN GONADAL RIDGE DEVELOPMENT

      Human genetics
    90. JAMES RS; JACOBS PA
      MOLECULAR STUDIES OF THE ETIOLOGY OF TRISOMY 8 IN SPONTANEOUS-ABORTIONS AND THE LIVEBORN POPULATION

      Human genetics
    91. ITTMANN MM
      LOSS OF HETEROZYGOSITY ON CHROMOSOME-10 AND CHROMOSOME-17 IN CLINICALLY LOCALIZED PROSTATE CARCINOMA

      The Prostate
    92. JIRICNY J
      MISMATCH REPAIR AND CANCER

      Cancer surveys
    93. DONNELLY AJ; PARTINGTON MW; RYAN AK; MULLEY JC
      REGIONAL LOCALIZATION OF 2 NONSPECIFIC X-LINKED MENTAL-RETARDATION GENES (MRX30 AND MRX31)

      American journal of medical genetics
    94. MILUNSKY JM; WYANDT HE; HUANG XL; KANG XZ; ELIAS ER; MILUNSKY A
      TRISOMY 15 MOSAICISM AND UNIPARENTAL DISOMY (UPD) IN A LIVEBORN INFANT

      American journal of medical genetics
    95. YIP B; CHAN V; CHAN TK
      A SEMIAUTOMATED METHOD FOR ANALYSIS OF INTRON-13 AND INTRON-22 DINUCLEOTIDE REPEAT POLYMORPHISMS OF THE FACTOR-VIII GENE

      Clinical and laboratory haematology
    96. TIMMERMAN V; DEJONGHE P; SPOELDERS P; SIMOKOVIC S; LOFGREN A; NELIS E; VANCE J; MARTIN JJ; VANBROECKHOVEN C
      LINKAGE AND MUTATION ANALYSIS OF CHARCOT-MARIE-TOOTH NEUROPATHY TYPE-2 FAMILIES WITH CHROMOSOMES 1P35-P36 AND XQ13

      Neurology
    97. SCULERATI N; ODDOUX C; CLAYTON CM; LIM JW; OSTER H
      HEARING-LOSS IN TURNER SYNDROME

      The Laryngoscope
    98. LATIL A; FOURNIER G; CUSSENOT O; LIDEREAU R
      DIFFERENTIAL CHROMOSOME ALLELIC IMBALANCE IN THE PROGRESSION OF HUMANPROSTATE-CANCER

      The Journal of urology
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/05/20 alle ore 18:24:15