THE OCULOCEREBROCUTANEOUS (DELLEMAN) SYNDROME

被引：50

作者：

ALGAZALI, LI

DONNAI, D

BERRY, SA

SAY, B

MUELLER, RF

机构：

[1] ST MARYS HOSP,DEPT MED GENET,MANCHESTER M13 0JH,LANCS,ENGLAND

[2] UNIV MINNESOTA,DEPT PEDIAT,DIV GENET,MINNEAPOLIS,MN 55455

[3] CHILDRENS MED CTR,H ALLEN CHAPMAN RES INST MED GENET,TULSA,OK

来源：

JOURNAL OF MEDICAL GENETICS | 1988年 / 25卷 / 11期

关键词：

D O I：

10.1136/jmg.25.11.773

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：773 / 778

页数：6

共 11 条

[1]

DELLEMAN JW, 1984, CLIN GENET, V25, P470

[2]

DELLEMAN JW, 1981, CLIN GENET, V19, P191

[3]

DUKEELDER S, 1983, SYSTEM OPHTHALMOLO 2, V3, P481

[4]

FERGUSON JW, 1984, CLIN GENET, V25, P464

[5] A NEW SYNDROME OF HEMANGIOMATOUS BRANCHIAL CLEFTS, LIP PSEUDOCLEFTS, AND UNUSUAL FACIAL APPEARANCE [J].

HALL, BD ;

DELORIMIER, A ;

FOSTER, LH .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (01) :135-138

[6] LETHAL GENES SURVIVING BY MOSAICISM - A POSSIBLE EXPLANATION FOR SPORADIC BIRTH-DEFECTS INVOLVING THE SKIN [J].

HAPPLE, R .

JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1987, 16 (04) :899-906

[7] BILATERAL BRANCHIAL CLEFT SINUSES ASSOCIATED WITH INTRAUTERINE AND POSTNATAL-GROWTH RETARDATION, PREMATURE AGING, AND UNUSUAL FACIAL APPEARANCE - A NEW SYNDROME WITH DOMINANT TRANSMISSION [J].

LEE, WK ;

ROOT, AW ;

FENSKE, N .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 11 (03) :345-352

[8]

Renard G., 1964, B MEM SOC FR OPHTALM, V77, P297

[9]

WARING GO, 1976, AM J OPHTHALMOL, V82, P714, DOI 10.1016/0002-9394(76)90008-8

[10] OCULOCEREBROCUTANEOUS SYNDROME [J].

WILSON, RD ;

TRAVERSE, L ;

HALL, JG ;

FLODMARK, CO ;

ROOTMAN, J .

AMERICAN JOURNAL OF OPHTHALMOLOGY, 1985, 99 (02) :142-148

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