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 authors phrase all words ' MATHEW CG' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 70 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Medhurst, AL; Huber, PAJ; Waisfisz, Q; de Winter, JP; Mathew, CG
      Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway

      HUMAN MOLECULAR GENETICS
    2. Hanson, H; Mathew, CG; Docherty, Z; Ogilvie, CM
      Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach

      CYTOGENETICS AND CELL GENETICS
    3. Hampe, J; Cuthbert, A; Croucher, PJP; Mirza, MM; Mascheretti, S; Fisher, S; Frenzel, H; King, K; Hasselmeyer, A; MacPherson, AJS; Bridger, S; van Deventer, S; Forbes, A; Nikolaus, S; Lennard-Jones, JE; Foelsch, UR; Krawczak, M; Lewis, C; Schreiber, S; Mathew, CG
      Association between insertion mutation in NOD2 gene and Crohn's disease inGerman and British populations

      LANCET
    4. Tipping, AJ; Pearson, T; Morgan, NV; Gibson, RA; Kuyt, LP; Havenga, C; Gluckman, E; Joenje, H; de Ravel, T; Jansen, S; Mathew, CG
      Molecular and genealogical evidence for a founder effect in Fanconi anemiafamilies of the Afrikaner population of South Africa

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    5. Hampe, J; Lynch, NJ; Daniels, S; Bridger, S; Macpherson, AJS; Stokkers, P; Forbes, A; Lennard-Jones, JE; Mathew, CG; Curran, ME; Schreiber, S
      Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease

      GUT
    6. Cleton-Jansen, AM; Callen, DF; Seshadri, R; Goldup, S; McCallum, B; Crawford, J; Powell, JA; Settasatian, C; van Beerendonk, H; Moerland, EW; Smit, VTBHM; Harris, WH; Millis, R; Morgan, NV; Barnes, D; Mathew, CG; Cornelisse, CJ
      Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions

      CANCER RESEARCH
    7. de Winter, JP; Rooimans, MA; van der Weel, L; van Berkel, CGM; Alon, N; Bosnoyan-Collins, L; de Groot, J; Zhi, Y; Waisfisz, Q; Pronk, JC; Arwert, F; Mathew, CG; Scheper, RJ; Hoatlin, ME; Buchwald, M; Joenje, H
      The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

      NATURE GENETICS
    8. Demuth, I; Wlodarski, M; Tipping, AJ; Morgan, NV; de Winter, JP; Thiel, M; Grasl, S; Schindler, D; D'Andrea, AD; Altay, C; Kayserili, H; Zatterale, A; Kunze, J; Ebell, W; Mathew, CG; Joenje, H; Sperling, K; Digweed, M
      Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

      EUROPEAN JOURNAL OF HUMAN GENETICS
    9. Olavesen, MG; Hampe, J; Mirza, MM; Saiz, R; Lewis, CM; Bridger, S; Teare, D; Easton, DF; Herrmann, T; Scott, G; Hirst, J; Sanderson, J; Hodgson, SV; Lee, J; MacPherson, A; Schreiber, S; Lennard-Jones, JE; Curran, ME; Mathew, CG
      Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease

      IMMUNOGENETICS
    10. Ellis, D; Greenman, J; Hodgson, S; McCall, S; Lalloo, F; Cameron, J; Izatt, L; Scott, G; Jacobs, C; Watts, S; Chorley, W; Perrett, C; Macdermot, K; Mohammed, S; Evans, G; Mathew, CG
      Low prevalence of germline BRCA1 mutations in early onset breast cancer without a family history

      JOURNAL OF MEDICAL GENETICS
    11. Faivre, L; Guardiola, P; Lewis, C; Dokal, I; Ebell, W; Zatterale, Z; Altay, C; Poole, J; Stones, D; Kwee, ML; van Weel-Sipman, M; Havenga, C; Morgan, N; de Winter, J; Digweed, M; Savoia, A; Pronk, J; de Ravel, T; Jansen, S; Joenje, H; Gluckman, E; Mathew, CG
      Association of complementation group and mutation type with clinical outcome in Fanconi anemia

      BLOOD
    12. Huber, PAJ; Medhurst, AL; Youssoufian, H; Mathew, CG
      Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    13. de Winter, JP; Leveille, F; van Berkel, CGM; Rooimans, MA; van der Weel, L; Steltenpool, J; Demuth, I; Morgan, NV; Alon, N; Bosnoyan-Collins, L; Lightfoot, J; Leegwater, PA; Waisfisz, Q; Komatsu, K; Arwert, F; Pronk, JC; Mathew, CG; Digweed, M; Buchwald, M; Joenje, H
      Isolation of a cDNA representing the Fanconi anemia complementation group E gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. Joenje, H; Levitus, M; Waisfisz, Q; D'Andrea, A; Garcia-Higuera, I; Pearson, T; van Berkel, CGM; Rooimans, MA; Morgan, N; Mathew, CG; Arwert, F
      Complementation analysis in Fanconi anemia: Assignment of the reference FA-H patient to group A

      AMERICAN JOURNAL OF HUMAN GENETICS
    15. Waisfisz, Q; Morgan, NV; Savino, M; de Winter, JP; van Berkel, CGM; Hoatlin, ME; Ianzano, L; Gibson, RA; Arwert, F; Savoia, A; Mathew, CG; Pronk, JC; Joenje, H
      Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism

      NATURE GENETICS
    16. Wijker, M; Morgan, NV; Herterich, S; van Berkel, CGM; Tipping, AJ; Gross, HJ; Gille, JJP; Pals, G; Savino, M; Altay, C; Mohan, S; Dokal, I; Cavenagh, J; Marsh, J; Van Weel, M; Ortega, JJ; Schuler, D; Samochatova, E; Karwacki, M; Bekassy, AN; Abecasis, M; Ebell, W; Kwee, ML; de Ravel, T; Gibson, RA; Gluckman, E; Arwert, F; Joenje, H; Savoia, A; Hoehn, H; Pronk, JC; Mathew, CG
      Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

      EUROPEAN JOURNAL OF HUMAN GENETICS
    17. Crawford, J; Ianzano, L; Savino, M; Whitmore, S; Cleton-Jansen, AM; Settasatian, C; d'Apolito, M; Seshadri, R; Pronk, JC; Auerbach, AD; Verlander, PC; Mathew, CG; Tipping, AJ; Doggett, NA; Zelante, L; Callen, DF; Savoia, A
      The PISSLRE gene: Structure, exon skipping, and exclusion as tumor suppressor in breast cancer

      GENOMICS
    18. Kupfer, G; Naf, D; Garcia-Higuera, I; Wasik, J; Cheng, A; Yamashita, T; Tipping, A; Morgan, N; Mathew, CG; D'Andrea, AD
      A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation

      EXPERIMENTAL HEMATOLOGY
    19. Hodgson, SV; Heap, E; Cameron, J; Ellis, D; Mathew, CG; Eeles, RA; Solomon, E; Lewis, CM
      Risk factors for detecting germline BRCA1 and BRCA2 founder mutations in Ashkenazi Jewish women with breast or ovarian cancer

      JOURNAL OF MEDICAL GENETICS
    20. Whittock, NV; Ashton, GHS; Mohammedi, R; Mellerio, JE; Mathew, CG; Abbs, SJ; Eady, RAJ; McGrath, JA
      Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresis

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    21. Mathew, CG
      DNA diagnostics: goals and challenges

      BRITISH MEDICAL BULLETIN
    22. Cleton-Jansen, AM; Moerland, EW; Pronk, JC; van Berkel, CGM; Apostolou, S; Crawford, J; Savoia, A; Auerbach, AD; Mathew, CG; Callen, DF; Cornelisse, CJ
      Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3

      BRITISH JOURNAL OF CANCER
    23. Catteau, A; Xu, CF; Brown, MA; Hodgson, S; Greenman, J; Mathew, CG; Dunning, AM; Solomon, E
      Identification of a C/G polymorphism in the promoter region of the BRCA1 gene and its use as a marker for rapid detection of promoter deletions

      BRITISH JOURNAL OF CANCER
    24. Hampe, J; Shaw, SH; Saiz, R; Leysens, N; Lantermann, A; Mascheretti, S; Lynch, NJ; MacPherson, AJS; Bridger, S; van Deventer, S; Stokkers, P; Morin, P; Mirza, MM; Forbes, A; Lennard-Jones, JE; Mathew, CG; Curran, ME; Schreiber, S
      Linkage of inflammatory bowel disease to human chromosome 6p

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. Morgan, NV; Tipping, AJ; Joenje, H; Mathew, CG
      High frequency of large intragenic deletions in the Fanconi anemia group Agene

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. Waisfisz, Q; Saar, K; Morgan, NV; Altay, C; Leegwater, PA; de Winter, JP; Komatsu, K; Evans, GR; Wegner, RD; Reis, A; Joenje, H; Arwert, F; Mathew, CG; Pronk, JC; Digweed, M
      The Fanconi anemia group E gene, FANCE, maps to chromosome 6p

      AMERICAN JOURNAL OF HUMAN GENETICS
    27. Hampe, J; Schreiber, S; Shaw, SH; Lau, KF; Bridger, S; Macpherson, AJS; Cardon, LR; Sakul, H; Harris, TJR; Buckler, A; Hall, J; Stokkers, P; van Deventer, SJH; Nurnberg, P; Mirza, MM; Lee, JCW; Lennard-Jones, JE; Mathew, CG; Curran, ME
      A genomewide analysis provides evidence for novel linkages in inflammatorybowel disease in a large European cohort

      AMERICAN JOURNAL OF HUMAN GENETICS
    28. LOTENFOE JR; KRUYT FAE; ZWEEKHORST MBM; PALS G; GIBSON RA; MATHEW CG; JOENJE H; ARWERT F
      EXON-6 SKIPPING IN THE FANCONI-ANEMIA-C GENE ASSOCIATED WITH A NONSENSE MISSENSE MUTATION (775C-]T) IN EXON-5 - THE FIRST EXAMPLE OF A NONSENSE MUTATION IN ONE EXON CAUSING SKIPPING OF ANOTHER DOWNSTREAM/

      Human mutation
    29. TAYLOR JE; THOMAS NH; LEWIS CM; ABBS SJ; RODRIGUES NR; DAVIES KE; MATHEW CG
      CORRELATION OF SMNT AND SMNC GENE COPY NUMBER WITH AGE-OF-ONSET AND SURVIVAL IN SPINAL MUSCULAR-ATROPHY

      European journal of human genetics
    30. WHITMORE SA; SETTASATIAN C; CRAWFORD J; LOWER KM; MCCALLUM B; SESHADRI R; CORNELISSE GJ; MOERLAND EW; CLETONJANSEN AM; TIPPING AJ; MATHEW CG; SAVNIO M; SAVOIA A; VERLANDER P; AUERBACH AD; VANBERKEL C; PRONK JC; DOGGETT NA; CALLEN DF
      CHARACTERIZATION AND SCREENING FOR MUTATIONS OF THE GROWTH-ARREST-SPECIFIC-11 (GAS11) AND C16ORF3 GENES AT 16Q24.3 IN BREAST-CANCER

      Genomics (San Diego, Calif.)
    31. WHITMORE SA; CRAWFORD J; APOSTOLOU S; EYRE H; BAKER E; LOWER KM; SETTASATIAN C; GOLDUP S; SESHADRI R; GIBSON RA; MATHEW CG; CLETONJANSEN AM; SAVOIA A; PRONK JC; AUERBACH AD; DOGGETT NA; SUTHERLAND GR; CALLEN DF
      CONSTRUCTION OF A HIGH-RESOLUTION PHYSICAL AND TRANSCRIPTION MAP OF CHROMOSOME 16Q124.3 - A REGION OF FREQUENT LOSS OF HETEROZYGOSITY IN SPORADIC BREAST-CANCER

      Genomics
    32. Hampe, J; Hermann, B; Bridger, S; MacPherson, AJS; Mathew, CG; Schreiber, S
      The interferon-gamma gene as a positional and functional candidate gene for inflammatory bowel disease

      INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
    33. MIRZA MM; LEE J; TEARE D; HUGOT JP; LAURENTPUIG P; COLOMBEL JF; HODGSON SV; THOMAS G; EASTON DF; LENNARDJONES JE; MATHEW CG
      EVIDENCE OF LINKAGE OF THE INFLAMMATORY BOWEL-DISEASE SUSCEPTIBILITY LOCUS ON CHROMOSOME-16 (IBD1) TO ULCERATIVE-COLITIS

      Journal of Medical Genetics
    34. LOTENFOE JR; KWEE ML; ROOIMANS MA; OOSTRA AB; VEERMAN AJP; VANWEEL M; PAULI RM; SHAHIDI NT; DOKAL I; ROBERTS I; ALTAY C; GLUCKMAN E; GIBSON RA; MATHEW CG; ARWERT F; JOENJE H
      SOMATIC MOSAICISM IN FANCONI-ANEMIA - MOLECULAR-BASIS AND CLINICAL-SIGNIFICANCE

      European journal of human genetics
    35. IANZANO L; DAPOLITO M; CENTRA M; SAVINO M; LEVRAN O; AUERBACH AD; CLETONJANSEN AM; DOGGETT NA; PRONK JC; TIPPING AJ; GIBSON RA; MATHEW CG; WHITMORE SA; APOSTOLOU S; CALLEN DF; ZELANTE L; SAVOIA A
      THE GENOMIC ORGANIZATION OF THE FANCONI-ANEMIA GROUP-A (FAA) GENE

      Genomics
    36. BARNICOAT AJ; WANG Q; TURK J; GREEN E; MATHEW CG; FLYNN G; BUCKLE V; HIRST M; DAVIES K; BOBROW M
      CLINICAL, CYTOGENETIC, AND MOLECULAR ANALYSIS OF 3 FAMILIES WITH FRAXE

      Journal of Medical Genetics
    37. TAYLOR J; ROSS S; ABBS S; MATHEW CG
      PRENATAL-DIAGNOSIS FOR AUTOSOMAL RECESSIVE CHILDHOOD-ONSET SPINAL MUSCULAR-ATROPHY - THE RESULTS OF 103 TESTS

      Journal of Medical Genetics
    38. BRETT PM; YIANNAKOU JY; CURTIS D; MATHEW CG; ROSENBRONSON S; CICLITIRA PJ
      LINKAGE STUDY OF CHROMOSOME-21 AND THE DOWNS DEPENDENT REGION IN THE GENETIC ETIOLOGY OF CELIAC-DISEASE

      Gastroenterology
    39. APOSTOLOU S; WHITMORE SA; CRAWFORD J; LENNON G; SUTHERLAND GR; CALLEN DF; IANZANO L; SAVINO M; DAPOLITO M; NOTARANGELO A; MEMEO E; PIEMONTESE MR; ZELANTE L; SAVOIA A; GIBSON RA; TIPPING AJ; MORGAN NV; HASSOCK S; JANSEN S; DERAVEL TJ; VANBERKEL C; PRONK JC; EASTON DF; MATHEW CG; LEVRAN O; VERLANDER PC; BATISH SD; ERLICH T; AUERBACH AD; CLETONJANSEN AM; MOERLAND EW; CORNELISSE CJ; DOGGETT NA; DEAVEN LL; MOYZIS RK
      POSITIONAL CLONING OF THE FANCONI-ANEMIA GROUP-A GENE

      Nature genetics
    40. GIBSON RA; MORGAN NV; GOLDSTEIN LH; PEARSON IC; KESTERTON IP; FOOT NJ; JANSEN S; HAVENGA C; PEARSON T; DERAVEL TJ; COHN RJ; MARQUES IM; DOKAL I; ROBERTS I; MARSH J; BALL S; MILNER RD; LLERENA JC; SAMOCHATOVA E; MOHAN SP; VASUDEVAN P; BIRJANDI F; HAJIANPOUR A; MURERORLANDO M; MATHEW CG
      NOVEL MUTATIONS AND POLYMORPHISMS IN THE FANCONI-ANEMIA GROUP C GENE

      Human mutation
    41. IWASE H; GREENMAN JM; BARNES DM; HODGSON S; BOBROW L; MATHEW CG
      SEQUENCE VARIANTS OF THE ESTROGEN-RECEPTOR (ER) GENE FOUND IN BREAST-CANCER PATIENTS WITH ER NEGATIVE AND PROGESTERONE-RECEPTOR POSITIVE TUMORS

      Cancer letters
    42. GIBSON RA; PRONK JC; SAVOIA A; MORGAN NV; WIJKER M; HASSOCK S; VETRIE D; OLAVESEN M; KENDALL E; FAURE S; WEISSENBACH J; DOGGETT NA; JOENJE H; ARWERT F; MATHEW CG
      LOCALIZATION OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-A GENE TO CHROMOSOME 16Q24.3

      Cytogenetics and cell genetics
    43. MATHEW CG; EASTON DF; LENNARDJONES JE
      HLA AND INFLAMMATORY BOWEL-DISEASE

      Lancet
    44. MATHEW CG; SOLOMON E; HODGSON SV
      BREAST-CANCER AND BRCA1 MUTATIONS

      The New England journal of medicine
    45. HUGOT JP; LAURENTPUIG P; GOWERROUSSEAU C; OLSON JM; LEE JC; BEAUGERIE L; NAOM I; DUPAS JL; VANGOSSUM A; ORHOLM M; BONAITIPELLIE C; WEISSENBACH J; MATHEW CG; LENNARDJONES JE; CORTOT A; COLOMBEL JF; THOMAS G
      MAPPING OF A SUSCEPTIBILITY LOCUS FOR CROHNS-DISEASE ON CHROMOSOME-16

      Nature
    46. YAU SC; BOBROW M; MATHEW CG; ABBS SJ
      ACCURATE DIAGNOSIS OF CARRIERS OF DELETIONS AND DUPLICATIONS IN DUCHENNE BECKER MUSCULAR-DYSTROPHY BY FLUORESCENT DOSAGE ANALYSIS/

      Journal of Medical Genetics
    47. YIANNAKOU JY; BRETT PM; CURTIS D; MATHEW CG; ROSENBRONSON S; CICLITIRA PJ
      GENETIC-LINKAGE STUDY OF THE ROLE OF THE T-CELL RECEPTOR GENES IN CELIAC-DISEASE

      Gastroenterology
    48. CAVENAGH JD; RICHARDSON DS; GIBSON RA; MATHEW CG; NEWLAND AC
      FANCONIS ANEMIA PRESENTING AS ACUTE MYELOID-LEUKEMIA IN ADULTHOOD

      British Journal of Haematology
    49. DOKAL I; CHASE A; MORGAN NV; COULTHARD S; HALL G; MATHEW CG
      POSITIVE DIEPOXYBUTANE TEST IN ONLY ONE OF 2 BROTHERS FOUND TO BE COMPOUND HETEROZYGOTES FOR FANCONI ANEMIA COMPLEMENTATION GROUP-C MUTATIONS

      British Journal of Haematology
    50. NAOM I; LEE J; FORD D; BOWMAN SJ; LANCHBURY JS; HARIS I; HODGSON SV; EASTON D; LENNARDLONES J; MATHEW CG
      ANALYSIS OF THE CONTRIBUTION OF HLA GENES TO GENETIC PREDISPOSITION IN INFLAMMATORY BOWEL-DISEASE

      American journal of human genetics
    51. PRONK JC; GIBSON RA; SAVOIA A; WIJKER M; MORGAN NV; MELCHIONDA S; FORD D; TEMTAMY S; ORTEGA JJ; JANSEN S; HAVENGA C; COHN RJ; DERAVEL TJ; ROBERTS I; WESTERVELD A; EASTON DF; JOENJE H; MATHEW CG; ARWERT F
      LOCALIZATION OF THE FANCONI-ANEMIA COMPLEMENTATION GROUP-A GENE TO CHROMOSOME 16Q24.3

      Nature genetics
    52. MCDOWELL GA; GAHL WA; STEPHENSON LA; SCHNEIDER JA; WEISSENBACH J; POLYMEROPOULOS MH; TOWN MM; VANTHOFF W; FARRALL M; MATHEW CG
      LINKAGE OF THE GENE FOR CYSTINOSIS TO MARKERS ON THE SHORT ARM OF CHROMOSOME-17

      Nature genetics
    53. BENNETT CP; BARNICOAT AJ; COTTER F; WANG Q; MATHEW CG
      A VARIANT OF WISKOTT-ALDRICH SYNDROME WITH NEPHROPATHY IS LINKED TO DXS255

      Journal of Medical Genetics
    54. WANG Q; GREEN E; BOBROW M; MATHEW CG
      A RAPID, NONRADIOACTIVE SCREENING-TEST FOR FRAGILE-X MUTATIONS AT THEFRAXA AND FRAXE LOCI

      Journal of Medical Genetics
    55. WANG Q; GREEN EP; BOBROW M; MATHEW CG
      SCREENING FOR THE FRAGILE-X A-MUTATION AND E-MUTATION BY AUTOMATED FLUORESCENT ANALYSIS

      Journal of Medical Genetics
    56. IWASE H; GREENMAN JM; BARNES DM; BOBROW L; HODGSON S; MATHEW CG
      LOSS OF HETEROZYGOSITY OF THE ESTROGEN-RECEPTOR GENE IN BREAST-CANCER

      British Journal of Cancer
    57. PERTL B; YAU SC; SHERLOCK J; DAVIES AF; MATHEW CG; ADINOLFI M
      RAPID MOLECULAR METHOD FOR PRENATAL DETECTION OF DOWNS-SYNDROME

      Lancet
    58. WANG Q; GREEN EP; MATHEW CG; BOBROW M
      NONRADIOACTIVE PCR BASED SCREENING FOR FRAGILE-X SYNDROME

      Journal of Medical Genetics
    59. GIBSON RA; FORD D; JANSEN S; SAVOIA A; HAVENGA C; MILNER RD; DERAVEL TJ; COHN RJ; BALL SE; ROBERTS I; LLERENA JC; VORECHOVSKY I; PEARSON T; BIRJANDI F; HUSSEIN SS; MURERORLANDO M; EASTON DF; MATHEW CG
      GENETIC-MAPPING OF THE FACC GENE AND LINKAGE ANALYSIS IN FANCONI-ANEMIA FAMILIES

      Journal of Medical Genetics
    60. NAOM IS; LEE JCW; FORD D; EASTON D; LENNARDJONES JE; MATHEW CG
      THE GENE FOR FAMILIAL CROHNS-DISEASE IS NOT LINKED TO THE MAJOR HISTOCOMPATIBILITY COMPLEX

      Gastroenterology
    61. VERLANDER PC; LIN JD; UDONO MU; ZHANG Q; GIBSON RA; MATHEW CG; AUERBACH AD
      MUTATION ANALYSIS OF THE FANCONI-ANEMIA GENE FACC

      American journal of human genetics
    62. GIBSON RA; SAVOIA A; BUCHWALD M; MATHEW CG
      ECORI RFLP IN THE FANCONI-ANEMIA COMPLEMENTATION GROUP-C GENE (FACC)

      Human molecular genetics
    63. GIBSON RA; HAJIANPOUR A; MURERORLANDO M; BUCHWALD M; MATHEW CG
      A NONSENSE MUTATION AND EXON SKIPPING IN THE FANCONI-ANEMIA GROUP-C GENE

      Human molecular genetics
    64. GIBSON RA; HAJIANPOUR A; ROBERTS RG; BUCHWALD M; MATHEW CG
      EXON STRUCTURE AND MUTATION ANALYSIS OF THE FANCONI-ANEMIA GROUP-C GENE

      Experimental hematology
    65. WANG Q; GREEN E; BARNICOAT A; GARRETT D; MULLARKEY M; BOBROW M; MATHEW CG
      CYTOGENETIC VERSUS DNA DIAGNOSIS IN ROUTINE REFERRALS FOR FRAGILE-X SYNDROME

      Lancet
    66. MURERORLANDO M; LLERENA JC; BIRJANDI F; GIBSON RA; MATHEW CG
      FACC GENE-MUTATIONS AND EARLY PRENATAL-DIAGNOSIS OF FANCONIS ANEMIA

      Lancet
    67. WALLIS GA; SYKES B; BYERS PH; MATHEW CG; VILJOEN D; BEIGHTON P
      OSTEOGENESIS IMPERFECTA TYPE-III - MUTATIONS IN THE TYPE-I COLLAGEN STRUCTURAL GENES, COL1A1 AND COL1A2, ARE NOT NECESSARILY RESPONSIBLE

      Journal of Medical Genetics
    68. NAOM IS; LEE JCW; HODGSON SVH; LENNARDJONES JE; MATHEW CG
      GENETIC-LINKAGE ANALYSIS OF THE HLA REGION IN INFLAMMATORY BOWEL-DISEASE

      Gastroenterology
    69. AUERBACH AD; LIN JD; UDONO MU; ZHANG Q; GIBSON RA; MATHEW CG; VERLANDER PC
      MUTATION ANALYSIS OF THE FANCONI-ANEMIA GENE FACC

      Blood
    70. VERLANDER PC; LIN JD; UDONO MU; GIBSON RA; MATHEW CG; SHERMAN SL; AUERBACH AD
      MUTATION AND LINKAGE ANALYSIS OF THE FANCONI-ANEMIA GENE FACC

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 08/08/20 alle ore 15:12:38