A NEWLY RECOGNIZED NEUROECTODERMAL SYNDROME OF FAMILIAL ALOPECIA, ANOSMIA, DEAFNESS, AND HYPOGONADISM

被引：32

作者：

JOHNSON, VP

MCMILLIN, JM

ACETO, T

BRUINS, G

机构：

[1] UNIV S DAKOTA,SCH MED,DEPT PEDIAT & ADOLESCENT MED,VERMILLION,SD 57069

[2] UNIV S DAKOTA,SCH MED,DEPT OBSTET & GYNECOL,VERMILLION,SD 57069

[3] UNIV S DAKOTA,SCH MED,DEPT INTERNAL MED,VERMILLION,SD 57069

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1983年 / 15卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320150316

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：497 / 506

页数：10

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[6]

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[7] FATHER-TO-SON TRANSMISSION OF HYPOGONADISM WITH ANOSMIA - KALLMANNS SYNDROME [J].

MERRIAM, GR ;

BEITINS, IZ ;

BODE, HH .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1977, 131 (11) :1216-1219

[8]

REMNICK H, 1970, EMBRYOLOGY FACE ORAL, P18

[9]

ROSEN SW, 1965, 47TH P M END SOC

[10]

SALTI IS, 1979, CAN MED ASSOC J, V121, P428

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