A MALFORMED NEWBORN WITH MONOSOMY 4QTER

被引：0
|
作者：
HISATOMI, T
ONOZUKA, Y
KUROKI, Y
机构：
[1] HLTH INSURANCE KAWASAKI,KAWASAKI,JAPAN
[2] KANAGAWA CHILDRENS MED CTR,YOKOHAMA,KANAGAWA,JAPAN
来源：
JAPANESE JOURNAL OF HUMAN GENETICS | 1982年 / 27卷 / 02期
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：165 / 165
页数：1
相关论文
共 50 条
  • [41] Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation
    Tinsa, F.
    Chebbi, Y.
    Meddeb, M.
    Bousnina, D.
    Boussetta, K.
    Bousnina, S.
    JOURNAL OF APPLIED GENETICS, 2009, 50 (03) : 289 - 291
  • [42] The management of severely malformed newborn infants: the case of conjoined twins
    Dickens, BM
    Cook, RJ
    INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2001, 73 (01) : 69 - 75
  • [43] PRENATAL-DIAGNOSIS OF A FETUS WITH PARTIAL MONOSOMY 7(Q34-]QTER) AND PARTIAL TRISOMY 18(Q21-]QTER)
    PLUCHON, E
    GIOVANGRANDI, Y
    LABBE, F
    LEBRIS, MJ
    COLLET, M
    BRETTES, JP
    RIVIERE, D
    RIVIERE, MR
    PRENATAL DIAGNOSIS, 1993, 13 (10) : 983 - 988
  • [44] A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere
    Thomas, N. S. T.
    Wiseman, K.
    Spurlock, G.
    MacDonald, M.
    Ustek, D.
    Upadhyaya, M.
    JOURNAL OF MEDICAL GENETICS, 2007, 44 (03) : 215 - 218
  • [45] DENOVO PARTIAL 2Q3 TRISOMY DISTAL 7P22 MONOSOMY IN A MALFORMED NEWBORN WITH 7P DELETION PHENOTYPE AND CRANIOSYNOSTOSIS
    FRYNS, JP
    HASPESLAGH, M
    AGNEESSENS, A
    VANDENBERGHE, H
    ANNALES DE GENETIQUE, 1985, 28 (01): : 45 - 48
  • [46] EVALUATION OF GENETIC-COUNSELING FOLLOWING THE BIRTH OF A MALFORMED NEWBORN
    IVES, EJ
    HENICK, P
    MORGAN, K
    HOLMES, TM
    PEDIATRIC RESEARCH, 1985, 19 (04) : A249 - A249
  • [47] COMPLETE TRISOMY-8 IN A POLY-MALFORMED NEWBORN
    MOERMAN, F
    FRYNS, JP
    GODDEERIS, P
    DEVLIEGER, H
    EGGERMONT, E
    LAUWERYNS, J
    VANDENBERGHE, H
    ACTA PAEDIATRICA BELGICA, 1979, 32 (04) : 283 - 285
  • [48] MEGACOLON AND DEFECTIVE NEUTROPHIL CHEMOTAXIS IN A PATIENT WITH MONOSOMY-7 (Q32-]QTER)
    SANCHEZCORONA, J
    HERNANDEZ, A
    RAMOSZEJEDA, R
    ROLON, A
    GARCIACRUZ, D
    CANTU, JM
    REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION, 1981, 33 (02): : 244 - 244
  • [49] A newborn with monosomy X in association with corpus callosum agenesis
    Cura, Duygu Onur
    Iscan, Burcin
    Gursoy, Semra
    Guleryuz, Handan
    Cankaya, Tufan
    Ozturk, Tulay
    Bozkaya, Ozlem Giray
    PEDIATRICS AND NEONATOLOGY, 2017, 58 (05): : 455 - 457
  • [50] Prenatal diagnosis of monosomy 4p14→pter and trisomy 11q25→qter:: clinical presentations and outcomes
    Peng, HH
    Wang, TH
    Chao, AS
    Chang, YL
    Chang, SD
    Soong, YK
    PRENATAL DIAGNOSIS, 2005, 25 (12) : 1133 - 1137
12345