Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'CHROMOSOME-5' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 390 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Crabtree, J; Wiltshire, T; Brunk, B; Zhao, SY; Schug, J; Stoeckert, CJ; Bucan, M
      High-resolution BAC-based map of the central portion of mouse chromosome 5

      GENOME RESEARCH
    2. Liao, PH; Lee, TL; Yang, LC; Yang, SH; Chen, SL; Chou, MY
      Adenomatous polyposis coli gene mutation and decreased wildtype p53 protein expression in oral submucous fibrosis: A preliminary investigation

      ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS
    3. Fenton, PA; Clarke, SEM; Owen, W; Hibbert, J; Hodgson, SV
      Cribriform variant papillary thyroid cancer: A characteristic of familial adenomatous polyposis

      THYROID
    4. Wang, CC; Hawken, RJ; Larson, E; Zhang, XX; Alexander, L; Rutherford, MS
      Generation and mapping of expressed sequence tags from virus-infected swine macrophages

      ANIMAL BIOTECHNOLOGY
    5. Howard, TD; Whittaker, PA; Zaiman, AL; Koppelman, GH; Xu, JF; Hanley, MT; Meyers, DA; Postma, DS; Bleecker, ER
      Identification and association of polymorphisms in the interleukin-13 genewith asthma and atopy in a Dutch population

      AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
    6. Witzel-Schlomp, K; Rittner, C; Schneider, PM
      The human complement C9 gene: structural analysis of the 5 ' gene region and genetic polymorphism studies

      EUROPEAN JOURNAL OF IMMUNOGENETICS
    7. Zhao, BH; Bepler, G
      Transcript map and complete genomic sequence for the 310 kb region of minimal allele loss on chromosome segment 11p15.5 in non-small-cell lung cancer

      ONCOGENE
    8. Kapitanovic, S; Cacev, T; Spaventi, R; Pavelic, K
      Submerged gel electrophoresis on Spreadex gels - a new method for APC genemutation detection

      JOURNAL OF MOLECULAR MEDICINE-JMM
    9. Kauppi, P; Lindblad-Toh, K; Sevon, P; Toivonen, HTT; Rioux, JD; Villapakkam, A; Laitinen, LA; Hudson, TJ; Kere, J; Laitinen, T
      Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma

      GENOMICS
    10. Lai, F; Godley, LA; Joslin, J; Fernald, AA; Liu, J; Espinosa, R; Zhao, ND; Pamintuan, L; Till, BG; Larson, RA; Qian, ZJ; Le Beau, MM
      Transcript map and comparative analysis of the 1.5-Mb commonly deleted segment of human 5q31 in malignant myeloid diseases with a del(5q)

      GENOMICS
    11. Abiaka, C; Al-Awadi, F; Al-Sayer, H; Gulshan, S; Behbehani, A; Farghally, M; Simbeye, A
      Serum antioxidant and cholesterol levels in patients with different types of cancer

      JOURNAL OF CLINICAL LABORATORY ANALYSIS
    12. Lezon-Geyda, K; Najfeld, V; Johnson, EM
      Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndromeand progression to acute myelogenous leukemia

      LEUKEMIA
    13. Wise, LH
      Inclusion of candidate region studies in meta-analysis using the genome screen meta-analysis method: Application to asthma data

      GENETIC EPIDEMIOLOGY
    14. Page, GP; Wilcox, MA; Occhiuto, J; Adak, S; Neuberg, D; Bajorunaite, R; George, V
      Comparison of the QTDT analysis for IgE in the CSGA data set

      GENETIC EPIDEMIOLOGY
    15. Kaffer, CR; Grinberg, A; Pfeifer, K
      Regulatory mechanisms at the mouse Igf2/H19 locus

      MOLECULAR AND CELLULAR BIOLOGY
    16. Cotter, PD; Musci, TJ
      Interphase FISH with chromosome-specific protelomere probes for rapid prenatal diagnosis in a reciprocal translocation carrier

      PRENATAL DIAGNOSIS
    17. Kammerer, CM; Cox, LA; Mahaney, MC; Rogers, J; Shade, RE
      Sodium-lithium countertransport activity is linked to chromosome 5 in baboons

      HYPERTENSION
    18. Lynch, HT; Thorson, AG; McComb, RD; Franklin, BA; Tinley, ST; Lynch, JF
      Familial adenomatous polyposis and extracolonic cancer

      DIGESTIVE DISEASES AND SCIENCES
    19. Chen, E; Cotter, PD; Cohen, RA; Lachman, RS
      Characterization of a long-term survivor with Stuve-Wiedemann syndrome andmosaicism of a supernumerary marker chromosome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Faderl, S; Gidel, C; Kantarjian, HM; Manshouri, T; Keating, M; Albitar, M
      Loss of heterozygosity on chromosome 5 in adults with acute lymphoblastic leukemia

      LEUKEMIA RESEARCH
    21. Shek, LPC; Tay, AHN; Chew, FT; Goh, DLM; Lee, BW
      Genetic susceptibility to asthma and atopy among Chinese in Singapore - linkage to markers on chromosome 5q31-33

      ALLERGY
    22. Erdel, M; Theurl, M; Meyer, M; Duba, HC; Utermann, G; Werner-Felmayer, G
      High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokinecluster by fiber-fluorescence in situ hybridization

      IMMUNOGENETICS
    23. Schweiger, A; Stern, D; Lohman, IC; Baldini, M; Martinez, FD; Halonen, M
      Differences in proliferation of the hematopoietic cell line TF-1 and cytokine production by peripheral blood leukocytes induced by 2 naturally occurring forms of human IL-3

      JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
    24. Munier, FL; Schorderet, DF
      Chromosome 5q31 linked Corneal Dystrophies: Outline of a new classification

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    25. Zauber, NP; Sabbath-Solitare, M; Marotta, SP; Zauber, AG; Bishop, DT
      Molecular changes in the Ki-ras and APC genes in colorectal adenomas and carcinomas arising in the same patient

      JOURNAL OF PATHOLOGY
    26. Mainardi, PC; Perfumo, C; Cali, A; Coucourde, G; Pastore, G; Cavani, S; Zara, F; Overhauser, J; Pierluigi, M; Bricarelli, FD
      Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

      JOURNAL OF MEDICAL GENETICS
    27. Silvia, OJ; Shellam, GR; Urosevic, N
      Innate resistance to flavivirus infection in mice controlled by Flv is nitric oxide-independent

      JOURNAL OF GENERAL VIROLOGY
    28. Berg, JN; Walter, JW; Thisanagayam, U; Evans, M; Blei, F; Waner, M; Diamond, AG; Marchuk, DA; Porteous, ME
      Evidence for loss of heterozygosity of 5q in sporadic haemangiomas: are somatic mutations involved in haemangioma formation

      JOURNAL OF CLINICAL PATHOLOGY
    29. Heinimann, K; Thompson, A; Locher, A; Furlanetto, T; Bader, E; Wolf, A; Meier, R; Walter, K; Bauerfeind, P; Marra, G; Muller, H; Foernzler, D; Dobbie, Z
      Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis

      CANCER RESEARCH
    30. Sakatani, T; Wei, M; Katoh, M; Okita, C; Wada, D; Mitsuya, K; Meguro, M; Ikeguchi, M; Ito, H; Tycko, B; Oshimura, M
      Epigenetic heterogeneity at imprinted loci in normal populations

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    31. Almasy, L; Porjesz, B; Blangero, J; Goate, A; Edenberg, HJ; Chorlian, DB; Kuperman, S; O'Connor, SJ; Rohrbaugh, J; Bauer, LO; Foroud, T; Rice, JP; Reich, T; Begleiter, H
      Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism

      AMERICAN JOURNAL OF HUMAN GENETICS
    32. Smith, MT; Rothman, N
      Biomarkers in the molecular epidemiology of benzene-exposed workers

      JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
    33. Mendes-da-Silva, P; Moreira, A; Duro-da-Costa, J; Matias, D; Monteiro, C
      Frequent loss of heterozygosity on chromosome 5 in non-small cell lung carcinoma

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    34. Sato, S; Nakamura, Y; Kaneko, T; Katoh, T; Asamizu, E; Kotani, H; Tabata, S
      Structural analysis of Arabidopsis thaliana chromosome 5. X. sequence features of the regions of 3,076,755 bp covered by sixty P1 and TAC clones

      DNA RESEARCH
    35. Chelsea, DM; Roberts, T; Cowell, JK
      A new region of synteny between human chromosome 1p22 and mouse chromosome5

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    36. Sanchez-Borges, N; Capriles-Hulett, A
      Atopy is a risk factor for non-steroidal anti-inflammatory drug sensitivity

      ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
    37. Srimatkandada, S; Dube, SK; Carmen, M; Bertino, JR
      Coamplification of 3-hydroxy-3-methylglutaryl coenzyme A reductase genes in methotrexate-resistant human leukemia cell lines

      ONCOLOGY RESEARCH
    38. Muller, S; van den Boom, D; Zirkel, D; Koster, H; Berthold, F; Schwab, M; Westphal, M; Zumkeller, W
      Retention of imprinting of the human apoptosis-related gene TSSC3 in humanbrain tumors

      HUMAN MOLECULAR GENETICS
    39. Paulsen, M; El-Maarri, O; Engemann, S; Strodicke, M; Franck, O; Davies, K; Reinhardt, R; Reik, W; Walter, J
      Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

      HUMAN MOLECULAR GENETICS
    40. Pollard, SL; Holland, PWH
      Evidence for 14 homeobox gene clusters in human genome ancestry

      CURRENT BIOLOGY
    41. Perard, L; Thomas, X; Jaumain, H; Theuil, G; Bret, M; Coronel, B; Charrin, C; Bouletreau, P
      T-cell lineage acute lymphoblastic leukemia with chromosome 5 abnormality in a patient with Crohn's disease and lipoid nephrosis

      ANNALS OF HEMATOLOGY
    42. Jordan, SF; Jackson, IJ
      A late wave of melanoblast differentiation and rostrocaudal migration revealed in patch and rump-white embryos

      MECHANISMS OF DEVELOPMENT
    43. Wang, YL; Saigoh, K; Osaka, H; Yamanishi, T; Suh, JG; Kiyosawa, H; Sakai, Y; Wakana, S; Wada, K
      YAC/BAC-based physical and transcript mapping around the gracile axonal dystrophy (gad) locus identifies Uchl1, Pmx2b, Atp3a2, and Hip2 genes

      GENOMICS
    44. Boultwood, J; Fidler, C; Strickson, AJ; Watkins, F; Kostrzewa, M; Jaju, RJ; Muller, U; Wainscoat, JS
      Transcription mapping of the 5q-syndrome critical region: Cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs

      GENOMICS
    45. Tarantino, LM; Feiner, L; Alavizadeh, A; Wiltshire, T; Hurle, B; Ornitz, DM; Webber, AL; Raper, J; Lengeling, A; Rowe, LB; Bucan, M
      A high-resolution radiation hybrid map of the proximal portion of mouse chromosome 5

      GENOMICS
    46. Medina, M; Marinescu, RC; Overhauser, J; Kosik, KS
      Hemizygosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome

      GENOMICS
    47. Viale, A; Courseaux, A; Presse, F; Ortola, C; Breton, C; Jordan, D; Nahon, JL
      Structure and expression of the variant melanin-concentrating hormone genes: Only PMCHL1 is transcribed in the developing human braid and encodes a putative protein

      MOLECULAR BIOLOGY AND EVOLUTION
    48. Stillman, WS; Varella-Garcia, M; Irons, RD
      The benzene metabolite, hydroquinone, selectively induces 5q31-and-7 in human CD34(+)CD19(-) bone marrow cells

      EXPERIMENTAL HEMATOLOGY
    49. Sato, M; Soma, M; Nakayama, T; Kanmatsuse, K
      Dopamine D1 receptor gene polymorphism is associated with essential hypertension

      HYPERTENSION
    50. Gorgoulis, VG; Mariatos, G; Manolis, EN; Zacharatos, P; Kotsinas, A; Liloglou, T; Vogiatzi, T; Tsagkaraki, A; Kokotas, S; Tsoli, E; Alchanatis, M; Sfikakis, PP; Asimacopoulos, PJ; Field, JK; Kittas, C
      Allelic imbalance at the 5q14 locus is associated with decreased apoptoticrate in non-small cell lung carcinomas (NSCLCs). Possible synergistic effect with p53 gene alterations on apoptosis

      LUNG CANCER
    51. Lehrer, S; McCurdy, LD; Stock, RG; Kornreich, R; Stone, NN; Eng, C
      Body mass, age, and the APC I1307K allele in Ashkenazi Jewish prostate cancer patients

      CANCER GENETICS AND CYTOGENETICS
    52. Brezinova, J; Zemanova, Z; Cermak, J; Michalova, K
      Fluorescence in situ hybridization confirmation of 5q deletions in patients with hematological malignancies

      CANCER GENETICS AND CYTOGENETICS
    53. Marinescu, RC; Mainardi, PC; Collins, MR; Kouahou, M; Coucourde, G; Pastore, G; Eaton-Evans, J; Overhauser, J
      Growth charts for cri-du-chat syndrome: An international collaborative study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    54. Spranger, S; Rommel, B; Jauch, A; Bodammer, R; Mehl, B; Bullerdiek, J
      Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. Braddock, SR; Henley, KM; Potter, KL; Nguyen, HG; Huang, THM
      Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21in a four-generation family

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. Van Buggenhout, GJCM; Pijkels, E; Holvoet, M; Schaap, C; Hamel, BCJ; Fryns, JP
      Cri du chat syndrome: Changing phenotype in older patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    57. Dicato, M; Berchem, G; Duhem, C; Ries, F
      The biology of colorectal cancer

      SEMINARS IN ONCOLOGY
    58. 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
    59. von Knobloch, R; Bugert, P; Jauch, A; Kalble, T; Kovacs, G
      Allelic changes at multiple regions of chromosome 5 are associated with progression of urinary bladder cancer

      JOURNAL OF PATHOLOGY
    60. Catchpoole, D; Smallwood, AV; Joyce, JA; Murrell, A; Lam, W; Tang, T; Munroe, D; Reik, W; Schofield, PN; Maher, ER
      Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome

      JOURNAL OF MEDICAL GENETICS
    61. Johnson, EI; Marinescu, RC; Punnett, HH; Tenenholz, B; Overhauser, J
      5p14 deletion associated with microcephaly and seizures

      JOURNAL OF MEDICAL GENETICS
    62. Hastings, RJ; Svennevik, EC; Setterfield, B; Wells, D; Delhanty, JDA; Mackinnon, H
      Deletion and duplication of the adenomatous polyposis coli gene resulting from an interchromosomal insertion involving 5(q22q23.3) in the father

      JOURNAL OF MEDICAL GENETICS
    63. Perfumo, C; Mainardi, PC; Cali, A; Coucourde, G; Zara, F; Cavani, S; Overhauser, J; Bricarelli, FD; Pierluigi, M
      The first three mosaic cri du chat syndrome patients with two rearranged cell lines

      JOURNAL OF MEDICAL GENETICS
    64. Koorey, D; Basha, NJ; Tomaras, C; Freiman, J; Robson, L; Smith, A
      Appendiceal carcinoma complicating adenomatous polyposis in a young woman with a de novo constitutional reciprocal translocation t(5;8)(q22;p23.1)

      JOURNAL OF MEDICAL GENETICS
    65. Tekeoglu, M; Tullu, A; Kaiser, WJ; Muehlbauer, FJ
      Inheritance and linkage of two genes that confer resistance to Fusarium wilt in chickpea

      CROP SCIENCE
    66. Schwienbacher, C; Angioni, A; Scelfo, R; Veronese, A; Calin, GA; Massazza, G; Hatada, I; Barbanti-Brodano, G; Negrini, M
      Abnormal RNA expression of 11p15 imprinted genes and kidney developmental genes in Wilms' tumor

      CANCER RESEARCH
    67. Westbrook, CA; Hsu, WT; Chyna, B; Litvak, D; Raza, A; Horrigan, SK
      Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia

      BRITISH JOURNAL OF HAEMATOLOGY
    68. Oya, M; Schulz, WA
      Decreased expression of p57(KIP2) mRNA in human bladder cancer

      BRITISH JOURNAL OF CANCER
    69. Horrigan, SK; Arbieva, ZH; Xie, HY; Kravarusic, J; Fulton, NC; Naik, H; Le, TT; Westbrook, CA
      Delineation of a minimal interval and identification of 9 candidates for atumor suppressor gene in malignant myeloid disorders on 5q31

      BLOOD
    70. Loh, EW; Smith, I; Murray, R; McLaughlin, M; McNulty, S; Ball, D
      Association between variants at the GABA(A)beta 2, GABA(A)alpha 6 and GABA(A)gamma 2 gene cluster and alcohol dependence in a Scottish population

      MOLECULAR PSYCHIATRY
    71. Zauber, NP; Sabbath-Solitaire, M; Marotta, SP; McMahon, L; Bishop, DT
      Comparison of allelic ratios from paired blood and paraffin-embedded normal tissue for use in a polymerase chain reaction to assess loss of heterozygosity

      MOLECULAR DIAGNOSIS
    72. Chouchane, L; Sfar, I; Bousaffara, R; El Kamel, A; Sfar, MT; Ismail, A
      A repeat polymorphism in interleukin-4 gene is highly associated with specific clinical phenotypes of asthma

      INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
    73. Rosenwasser, LJ
      Promoter polymorphism in the candidate genes, IL-4, IL-9, TGF-beta 1, for atopy and asthma

      INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
    74. Johannes, C; Chudoba, I; Obe, G
      Analysis of X-ray-induced aberrations in human chromosome 5 using high-resolution multicolour banding FISH (mBAND)

      CHROMOSOME RESEARCH
    75. Tutois, S; Cloix, C; Cuvillier, C; Espagnol, MC; Lafleuriel, J; Picard, G; Tourmente, S
      Structural analysis and physical mapping of a pericentromeric region of chromosome 5 of Arabidopsis thaliana

      CHROMOSOME RESEARCH
    76. Lee, MP; Brandenburg, S; Landes, GM; Adams, M; Miller, G; Feinberg, AP
      Two novel genes in the center of the 11p15 imprinted domain escape genomicimprinting

      HUMAN MOLECULAR GENETICS
    77. John, RM; Hedges, M; Little, P; Barton, SC; Surani, MA
      A human p57(KIP2) transgene is not activated by passage through the maternal mouse germline

      HUMAN MOLECULAR GENETICS
    78. Bradley, ANM
      The contribution of molecular genetics to the understanding and managementof cancer: potential future applications and implications for nurses

      EUROPEAN JOURNAL OF CANCER CARE
    79. Martins, C; Jin, Y; Jin, C; Wennerberg, J; Hoglund, M; Mertens, F
      Fluorescent in situ hybridisation (FISH) characterisation of pericentromeric breakpoints on chromosome 5 in head and neck squamous cell carcinomas

      EUROPEAN JOURNAL OF CANCER
    80. Ying, HC; Hurle, B; Wang, YX; Bohne, BA; Wuerffel, MK; Ornitz, DM
      High-resolution mapping of tlt, a mouse mutant lacking otoconia

      MAMMALIAN GENOME
    81. Wurthner, J; Rump, LC; Grotz, W; Engelhardt, R; Lubbert, M
      Management of acute myeloid leukaemia following myelodysplastic syndrome in a kidney graft recipient

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    82. Puechberty, J; Laurent, AM; Gimenez, S; Billault, A; Brun-Laurent, ME; Calenda, A; Marcais, B; Prades, C; Ioannou, P; Yurov, Y; Roizes, G
      Genetic and physical analyses of the centromeric and pericentromeric regions of human chromosome 5: Recombination across 5cen

      GENOMICS
    83. Turner, M; Mukai, Y; Leroy, P; Charef, B; Appels, R; Rahman, S
      The Ha locus of wheat: Identification of a polymorphic region for tracing grain hardness in crosses

      GENOME
    84. Dizier, MH; Sandford, A; Walley, A; Philippi, A; Cookson, W; Demenais, F
      Indication of linkage of serum IgE levels to the interleukin-4 gene and exclusion of the contribution of the (-590 C to T) interleukin-4 promoter polymorphism to IgE variation

      GENETIC EPIDEMIOLOGY
    85. Bohm, M; Schmidt, C; Wieland, I; Leclerc, N; Allhoff, EP
      Membrane-based laser microdissection in molecular oncology

      ONKOLOGIE
    86. Leclerc, D; Odievre, MH; Wu, Q; Wilson, A; Huizenga, JJ; Rozen, R; Scherer, SW; Gravel, RA
      Molecular cloning, expression and physical mapping of the human methioninesynthase reductase gene

      GENE
    87. Bodmer, W
      Familial adenomatous polyposis (FAP) and its gene, APC

      CYTOGENETICS AND CELL GENETICS
    88. Skinnider, BF; Connors, JM; Sutcliffe, SB; Gascoyne, RD
      Anaplastic large cell lymphoma: A clinicopathologic analysis

      HEMATOLOGICAL ONCOLOGY
    89. Shaoul, R; Papsin, B; Cutz, E; Durie, P
      Congenital cholesteatoma in a child carrying a gene mutation for adenomatous polyposis coli

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    90. Czembor, JH; Johnston, MR
      Resistance to powdery mildew in selections from Tunisian landraces of barley

      PLANT BREEDING
    91. Eason, DE; Shepherd, AT; Blanck, G
      Interferon regulatory factor 1 tryptophan 11 to arginine point mutation abolishes DNA binding

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    92. Chataway, J; Sawcer, S; Sherman, D; Hobart, M; Fernie, B; Coraddu, F; Feakes, R; Broadley, S; Gray, J; Hywel, BJD; Jones, HB; Clayton, D; Goodfellow, PN; Compston, A
      No evidence for association of multiple sclerosis with the complement factors C6 and C7

      JOURNAL OF NEUROIMMUNOLOGY
    93. Kojima, H; Ohmori, O; Shinkai, T; Terao, T; Suzuki, T; Abe, H
      Dopamine D1 receptor gene polymorphism and schizophrenia in Japan

      AMERICAN JOURNAL OF MEDICAL GENETICS
    94. Pilarski, RT; Brothman, AR; Benn, P; Rosengren, SS
      Attenuated familial adenomatous polyposis in a man with an interstitial deletion of chromosome arm 5q

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. Marinescu, RC; Mamunes, P; Kline, AD; Schmidt, J; Rojas, K; Overhauser, J
      Variability in a family with an insertion involving 5p

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. Marinescu, RC; Johnson, EI; Dykens, EM; Hodapp, RM; Overhauser, J
      No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    97. Mowat, D; Jauch, A; Robson, L; Smith, A
      Duplication within chromosome 5q characterized by fluorescence in situ hybridization

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. Kramer, RL; Feldman, B; Ebrahim, SAD; Kasperski, SB; Johnson, MP; Evans, MI
      Molecular cytogenetic analysis of a de novo 5q31q33 deletion associated multiple congenital anomalies: Case report

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. Kjaer, I; Niebuhr, E
      Studies of the cranial base in 23 patients with cri-du-chat syndrome suggest a cranial developmental field involved in the condition

      AMERICAN JOURNAL OF MEDICAL GENETICS
    100. Walter, JW; Blei, F; Anderson, JL; Orlow, SJ; Speer, MC; Marchuk, DA
      Genetic mapping of a novel familial form of infantile hemangioma

      AMERICAN JOURNAL OF MEDICAL GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 20:18:01