TRISOMY OF DISTAL 3RD OF LONG ARM OF CHROMOSOME 10 - REPORT OF A NEW CASE DUE TO A FAMILIAL TRANSLOCATION T (10-18) (Q24-P11)

被引：0
|
作者：
FORABOSCO, A
BERNASCONI, S
GIOVANNELLI, G
DUTRILLAUX, B
机构：
[1] IST ANAT UMANA NORM,MODENA,ITALY
[2] IST CLIN PEDIAT,PARMA,ITALY
[3] INST PROGENESE,PARIS,FRANCE
来源：
HELVETICA PAEDIATRICA ACTA | 1975年 / 30卷 / 03期
关键词：
D O I：
暂无
中图分类号：
B844 [发展心理学（人类心理学）];
学科分类号：
040202 ;
摘要：
引用
收藏
页码：289 / 295
页数：7
相关论文
共 39 条
  • [21] NEW CASE OF TRISOMY FOR DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9-13)(P21-Q21)
    JOTTERAND, M
    JUILLARD, E
    HUMAN GENETICS, 1976, 33 (03) : 213 - 222
  • [22] A FAMILIAL MCA/MR SYNDROME DUE TO TRANSLOCATION T(10-16)(Q26-P13.1) - REPORT OF 6 CASES
    BOFINGER, MK
    OPITZ, JM
    SOUKUP, SW
    EKBLOM, LS
    PHILLIPS, S
    DANIEL, A
    GREENE, EW
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1991, 38 (01): : 1 - 8
  • [23] Partial trisomy of distal 5q and partial monosomy of Xp as a result of mating between two translocation carriers: a female with a balanced translocation t(X;5)(p11;q31) and a male with a der(13;14)(q10;q10) - a case report and a family study
    Wysocka, B
    Brozek, I
    Wierzba, J
    Kardas, I
    Wozniak, A
    Kowalczyk, J
    Balcerska, A
    Limon, J
    ANNALES DE GENETIQUE, 2002, 45 (03): : 143 - 146
  • [24] Acute myeloid leukemia with t(10; 17)(p13;q12) chromosome translocation: a case report and literature review
    Li, Lu
    Zhou, Fan
    Hou, Jian
    AMERICAN JOURNAL OF BLOOD RESEARCH, 2012, 2 (04): : 265 - 268
  • [25] LOCALIZATION OF THE HUMAN NCAM GENE TO BAND-Q23 OF CHROMOSOME-11 - THE 3RD GENE CODING FOR A CELL-INTERACTION MOLECULE MAPPED TO THE DISTAL PORTION OF THE LONG ARM OF CHROMOSOME-11
    NGUYEN, C
    MATTEI, MG
    MATTEI, JF
    SANTONI, MJ
    GORIDIS, C
    JORDAN, BR
    JOURNAL OF CELL BIOLOGY, 1986, 102 (03): : 711 - 715
  • [26] INTER-CHROMOSOMAL DUPLICATION FOR SHORT ARM OF CHROMOSOME NO 9 - REPORT OF 3 CASES DUE TO A FAMILIAL TRANSLOCATION T(9-11) AND ONE CASE WITH A DENOVO 47, XX, + 9P KARYOTYPE
    LIN, CC
    HOLMAN, G
    SEWELL, L
    BOWEN, P
    BIEDERMAN, B
    JOURNAL OF MENTAL DEFICIENCY RESEARCH, 1977, 21 (DEC): : 309 - 320
  • [27] Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3-q23);: report of familial cryptic chromosome t(18q; 10p) translocations
    Dostal, A.
    Linnankivi, T.
    Somer, M.
    Kahkonen, M.
    Litzman, J.
    Tienari, P.
    INTERNATIONAL JOURNAL OF IMMUNOGENETICS, 2007, 34 (03) : 143 - 147
  • [28] A SEVERELY MENTALLY AND MOTOR RETARDED GIRL WITH MONOSOMY 3pter→p25 AND TRISOMY 8q24→qter DUE TO A FAMILIAL RECIPROCAL TRANSLOCATION t(3;8)(p25;q24)
    Balci, S.
    Aypar, E.
    Beksac, M. S.
    Bartsch, O.
    GENETIC COUNSELING, 2009, 20 (02): : 125 - 132
  • [29] ACROCEPHALOPOLYSYNDACTYLY, PENTALOGY OF FALLOT, AND HYPOACUSIS IN A PATIENT WITH A DENOVO RECIPROCAL TRANSLOCATION INVOLVING THE SHORT ARM OF CHROMOSOME-1 AND THE LONG ARM OF CHROMOSOME-18-46,XX,T(1-18)(P31-Q11)
    WARD, J
    VIETO, E
    LEE, D
    AROSEMENA, G
    JOURNAL OF MEDICAL GENETICS, 1993, 30 (05) : 438 - 439
  • [30] A NEW CASE OF MONOSOMY FOR 17Q25-]QTER DUE TO A MATERNAL TRANSLOCATION [T(3 17) (P12 Q24)]
    LUKE, S
    BENNETT, HS
    PITTER, JH
    VERMA, RS
    ANNALES DE GENETIQUE, 1992, 35 (01): : 48 - 50
1234