学术探索
学术期刊
新闻热点
数据分析
智能评审

HOLOPROSENCEPHALY AND CYTOGENETIC FINDINGS - FURTHER INFORMATION

被引：11
作者：
COHEN, MM
机构：
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 34卷 / 02期
关键词：
D O I：
10.1002/ajmg.1320340229
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：265 / 265
页数：1
相关论文
共 9 条
  • [1] ATKIN J F, 1988, American Journal of Human Genetics, V43, pA36
  • [2] COHEN MM, 1989, IN PRESS TERATOLOGY
  • [3] FAMILIAL AGNATHIA-HOLOPROSENCEPHALY CAUSED BY AN INHERITED UNBALANCED TRANSLOCATION AND NOT AUTOSOMAL RECESSIVE INHERITANCE
    KRASSIKOFF, N
    SEKHON, GS
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 34 (02): : 255 - 257
  • [4] HOLOPROSENCEPHALY - ASSOCIATION WITH INTERSTITIAL DELETION OF 2P AND REVIEW OF THE CYTOGENETIC LITERATURE
    MUNKE, M
    EMANUEL, BS
    ZACKAI, EH
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (04): : 929 - 938
  • [5] FAMILIAL AGNATHIA HOLOPROSENCEPHALY
    PAULI, RM
    PETTERSEN, JC
    ARYA, S
    GILBERT, EF
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (04): : 677 - 698
  • [6] WHAT IS THE INCIDENCE OF HOLOPROSENCEPHALY
    SAUNDERS, ES
    SHORTLAND, D
    DUNN, PM
    [J]. JOURNAL OF MEDICAL GENETICS, 1984, 21 (01) : 21 - 26
  • [7] SHANKS D E, 1988, American Journal of Human Genetics, V43, pA122
  • [8] HOLOPROSENCEPHALY, VENTRICULAR SEPTAL-DEFECT, AND POSTAXIAL POLYDACTYLY IN A HUMAN-EMBRYO
    SHIOTA, K
    TANIMURA, T
    [J]. JOURNAL OF MEDICAL GENETICS, 1988, 25 (07) : 502 - 503
  • [9] UNKNOWN SYNDROME - HOLOPROSENCEPHALY, CONGENITAL HEART-DEFECTS, AND POLYDACTYLY
    YOUNG, ID
    MADDERS, DJ
    [J]. JOURNAL OF MEDICAL GENETICS, 1987, 24 (11) : 714 - 715
1