CHROMOSOME-ABNORMALITIES IN AND PATHOGENESIS OF KALLMANN SYNDROME

被引：3

作者：

BICK, D ^{[1
]}

BALLABIO, A ^{[1
]}

机构：

[1] BAYLOR UNIV,INST MOLEC GENET,HOUSTON,TX 77030

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 37卷 / 02期

关键词：

D O I：

10.1002/ajmg.1320370236

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：298 / 298

页数：1

共 7 条

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[2] CHROMOSOME ABNORMALITY IN KALLMANN SYNDROME [J].

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[3] MALE INFANT WITH ICHTHYOSIS, KALLMANN SYNDROME, CHONDRODYSPLASIA PUNCTATA, AND AN XP CHROMOSOME DELETION [J].

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[5]

MEITINGER T, 1989, American Journal of Human Genetics, V45, pA151

[6] LUTEINIZING-HORMONE-RELEASING HORMONE (LHRH)-EXPRESSING CELLS DO NOT MIGRATE NORMALLY IN AN INHERITED HYPOGONADAL (KALLMANN) SYNDROME [J].

SCHWANZELFUKUDA, M ;

BICK, D ;

PFAFF, DW .

MOLECULAR BRAIN RESEARCH, 1989, 6 (04) :311-326

[7] ORIGIN OF LUTEINIZING-HORMONE-RELEASING HORMONE NEURONS [J].

SCHWANZELFUKUDA, M ;

PFAFF, DW .

NATURE, 1989, 338 (6211) :161-164

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