GENETIC-HETEROGENEITY OF THE ICHTHYOSIS, HYPOGONADISM, MENTAL-RETARDATION, AND EPILEPSY SYNDROME - CLINICAL AND BIOCHEMICAL INVESTIGATIONS ON 2 PATIENTS WITH RUD SYNDROME AND REVIEW OF THE LITERATURE

被引：33

作者：

MUNKE, M

KRUSE, K

GOOS, M

ROPERS, HH

TOLKSDORF, M

机构：

[1] UNIV KIEL,DEPT PEDIAT,D-2300 KIEL 1,FED REP GER

[2] UNIV KIEL,DEPT DERMATOL,D-2300 KIEL 1,FED REP GER

[3] UNIV FREIBURG,INST HUMAN GENET & ANTHROPOL,D-7800 FREIBURG,FED REP GER

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 1983年 / 141卷 / 01期

关键词：

D O I：

10.1007/BF00445661

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：8 / 13

页数：6

共 42 条

[11]

Jobsis A.C., 1976, NEDERLANDSCH TIJDSCH, V120, P1980

[12]

KISSEL P, 1973, J GENET HUM, V21, P15

[13]

LABRISSEAU A, 1982, NEUROGENETICS, V13, P95

[14]

Loza-Tulimowska M, 1971, Pol Tyg Lek, V26, P314

[15]

LYNCH HT, 1960, AM J HUM GENET, V12, P440

[16]

MacGillivray RC, 1954, AM J MENT DEF, V59, P67

[17] REGIONAL ASSIGNMENT OF THE GENE LOCUS FOR STEROID SULFATASE [J].

MULLER, CR ;

WESTERVELD, A ;

MIGL, B ;

FRANKE, W ;

ROPERS, HH .

HUMAN GENETICS, 1980, 54 (02) :201-204

[18] A UNIQUE CASE OF TRICHORRHEXIS NODOSA - BAMBOO HAIRS [J].

NETHERTON, EW .

ARCHIVES OF DERMATOLOGY, 1958, 78 (04) :483-487

[19]

Nissley P S, 1971, Birth Defects Orig Artic Ser, V7, P246

[20]

PASSWELL J, 1973, J PEDIATR-US, V82, P466

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