4P TRISOMY SYNDROME DUE TO DER(17) T(4-17)

被引:0
|
作者
SHAH, HO
RAMESH, KH
SHERMAN, J
LIN, JH
VERMA, RS
机构
[1] SUNY HLTH SCI CTR,BROOKLYN,NY 11203
[2] NASSAU CTY MED CTR,E MEADOW,NY 11554
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:1808 / 1808
页数:1
相关论文
共 50 条
  • [21] Book I, dd. 4-17
    不详
    GIORNALE CRITICO DELLA FILOSOFIA ITALIANA, 2020, 16 (02) : 405 - 407
  • [22] Partial trisomy 4p and Brachmann-de Lange syndrome
    Fryns, JP
    AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 95 (04): : 406 - 406
  • [23] TRISOMY 4P AND DELETION 4P- IN A FAMILY HAVING A TRANSLOCATION, T(4P--12P+)
    MORTIMER, JG
    CHEWINGS, W
    MIETHKE, P
    SMITH, GF
    HUMAN HEREDITY, 1978, 28 (02) : 132 - 140
  • [24] CLINICAL MANIFESTATIONS OF PARTIAL TRISOMY 4p
    Demirhan, O.
    Ozgunen, F. T.
    Tastemir, D.
    BALKAN JOURNAL OF MEDICAL GENETICS, 2010, 13 (02) : 61 - 63
  • [25] NEW CASE OF PARTIAL 4P TRISOMY
    CRISALLI, M
    MONTEVERDE, R
    BONIOLI, E
    VIANELLO, MG
    JOURNAL DE GENETIQUE HUMAINE, 1975, 23 : 96 - 96
  • [26] A Rare Chromosomal Disorder, Trisomy 4p
    Hepokur, Merve Nur
    Tatli, Zeynep Uzan
    Direk, Gul
    Akin, Leyla
    Hatipoglu, Nihal
    Kendirci, Mustafa
    Kurtoglu, Selim
    HORMONE RESEARCH IN PAEDIATRICS, 2018, 90 : 467 - 467
  • [27] TRISOMY 4P - 3 NEW OBSERVATIONS
    GIRAUD, F
    MATTEI, JF
    MATTEI, MG
    AYME, S
    BERNARD, R
    HUMANGENETIK, 1975, 30 (02): : 99 - 108
  • [28] COMBINED TRISOMY-1Q AND MONOSOMY-17P DUE TO TRANSLOCATION T(1-17) IN A PATIENT WITH MYELODYSPLASTIC SYNDROME
    MAMAEV, N
    MAMAEVA, SE
    PAVLOVA, VA
    PATTERSON, D
    CANCER GENETICS AND CYTOGENETICS, 1988, 35 (01) : 21 - 25
  • [29] A case of partial trisomy 4p syndrome presenting as severe hydronephrosis in utero
    Neas, KR
    Chia, N
    Clarke, M
    Peters, G
    Adès, LC
    CLINICAL DYSMORPHOLOGY, 2003, 12 (03) : 179 - 181
  • [30] ATR-16 due to a chromosomal rearrangement involving partial 4p trisomy
    Titomanlio, L
    De Brasi, D
    Fabbrini, F
    Genesio, R
    Conti, A
    Pecoraro, L
    Tardi, M
    Di Stefano, C
    Melis, D
    Del Giudice, E
    Sabastio, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 283 - 283