CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES - AUTOSOMAL DOMINANT PHENOTYPE IN A LARGE AMISH KINDRED

被引:81
作者
JACKSON, CE
WEISS, L
REYNOLDS, WA
FORMAN, TF
PETERSON, JA
机构
[1] HENRY FORD HOSP, DEPT RADIOL, CYTOGENET LAB, DETROIT, MI 48202 USA
[2] ELKHART CLIN, DEPT PEDIAT, ELKHART, IN USA
[3] HENRY FORD HOSP, GENET COUNSELING CLIN, DETROIT, MI 48202 USA
[4] HENRY FORD HOSP, DEPT MED, CYTOGENET LAB, DETROIT, MI 48202 USA
[5] HENRY FORD HOSP, DEPT PEDIAT, CYTOGENET LAB, DETROIT, MI 48202 USA
关键词
D O I
10.1016/S0022-3476(76)81050-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:963 / 968
页数:6
相关论文
共 6 条
[1]  
Cohen M M Jr, 1975, Birth Defects Orig Artic Ser, V11, P137
[2]   CRANIOSYNOSTOSIS IN AMISH [J].
CROSS, HE ;
OPITZ, JM .
JOURNAL OF PEDIATRICS, 1969, 75 (6P1) :1037-&
[3]  
MCKUSICK VA, 1969, PERSPECT BIOL MED, V12, P298
[4]  
MCKUSICK VA, 1975, MENDELIAN INHERITANC, P4
[5]  
PFEIFFER R A, 1964, Z Kinderheilkd, V90, P301, DOI 10.1007/BF00447500
[6]  
POZNANSKI AK, IN PRESS