A GENETIC FOLLOW-UP-STUDY OF 64 PATIENTS WITH THE PIERRE ROBIN COMPLEX

被引：56

作者：

SHEFFIELD, LJ ^{[1
]}

REISS, JA ^{[1
]}

STROHM, K ^{[1
]}

GILDING, M ^{[1
]}

机构：

[1] ADELAIDE CHILDRENS HOSP, MED GENET & EPIDEMIOL UNIT, N ADELAIDE, SA 5006, AUSTRALIA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 01期

关键词：

D O I：

10.1002/ajmg.1320280105

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：25 / 36

页数：12

共 16 条

[1] THE ROBIN SEQUENCE AS A CONSEQUENCE OF MALFORMATION, DYSPLASIA, AND NEUROMUSCULAR SYNDROMES
CAREY, JC
FINEMAN, RM
ZITER, FA
[J]. JOURNAL OF PEDIATRICS, 1982, 101 (05) : 858 - 864
[2] DEGROUCHY J, 1984, CLIN ATLAS HUMAN CHR, P200
[3] DENNISON WM, 1965, PEDIATRICS, V36, P336
[4] GORLIN RJ, 1976, SYNDROMES HEAD NECK, P132
[5] U-SHAPED PALATAL DEFECT IN ROBIN ANOMALAD - DEVELOPMENTAL AND CLINICAL RELEVANCE
HANSON, JW
SMITH, DW
[J]. JOURNAL OF PEDIATRICS, 1975, 87 (01) : 30 - 33
[6] HERRMAN J, 1975, BIRTH DEFECTS, V11, P77
[7] THE WAGNER-STICKLER SYNDROME - A STUDY OF 22 FAMILIES
LIBERFARB, RM
HIROSE, T
HOLMES, LB
[J]. JOURNAL OF PEDIATRICS, 1981, 99 (03) : 394 - 399
[8] THE BRACHMANN-DELANGE SYNDROME
OPITZ, JM
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (01): : 89 - 102
[9] OPITZ JM, 1972, NEW ENGL J MED, V286, P546
[10] PASYAYAN HM, 1984, CLEFT PALATE J, V21, P270