POSSIBLE WAARDENBURG SYNDROME WITH GASTROINTESTINAL ANOMALIES

被引：6

作者：

NUTMAN, J

STEINHERZ, R

SIVAN, Y

GOODMAN, RM

机构：

[1] BEILINSON MED CTR,DEPT PEDIAT A,IL-49100 PETACH TIKVA,ISRAEL

[2] CHAIM SHEBA MED CTR,DEPT HUMAN GENET,IL-52621 TEL HASHOMER,ISRAEL

来源：

关键词：

D O I：

10.1136/jmg.23.2.175

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：175 / 178

页数：4

共 50 条

[21] A PEDIGREE OF BINOCULAR HETEROCHROMIA IRIDIS ASSOCIATED WITH OTHER ANOMALIES (WAARDENBURG-KLEIN SYNDROME)
BASILE, R
JOURNAL DE GENETIQUE HUMAINE, 1965, 14 (2-3): : 87 - +
[22] What syndrome is this? Waardenburg syndrome
Cambiaghi, S
Cavalli, R
Legnani, C
Gelmetti, C
PEDIATRIC DERMATOLOGY, 1998, 15 (03) : 235 - 237
[23] HOMOZYGOSITY FOR WAARDENBURG SYNDROME
ZLOTOGORA, J
LERER, I
BARDAVID, S
ERGAZ, Z
ABELIOVICH, D
AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 56 (05) : 1173 - 1178
[24] HETEROGENEITY IN WAARDENBURG SYNDROME
HAGEMAN, MJ
DELLEMAN, JW
AMERICAN JOURNAL OF HUMAN GENETICS, 1977, 29 (05) : 468 - 485
[25] A family with Waardenburg syndrome
Denli, YG
Yücel, A
Günasti, S
Homan, S
Durdu, M
Süleymanova, D
JOURNAL OF DERMATOLOGY, 2004, 31 (05): : 434 - 436
[26] WAARDENBURG SYNDROME AND MENINGOCELE
BEGLEITER, ML
HARRIS, DJ
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 44 (04): : 541 - 541
[27] Waardenburg syndrome 2
Garg, Uma
Surana, Ritesh
INDIAN JOURNAL OF OTOLOGY, 2012, 18 (04) : 220 - 222
[28] WAARDENBURG SYNDROME AND MENINGOMYELOCELE
MOLINE, ML
SANDLIN, C
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (01): : 126 - 126
[29] FAMILY OF WAARDENBURG SYNDROME
OHKURA, K
ORITA, Y
MATSUDA, T
FUKUHARA, T
JAPANESE JOURNAL OF GENETICS, 1962, 37 (05): : 406 - &
[30] POLYSPLENIA SYNDROME - SPECTRUM OF GASTROINTESTINAL CONGENITAL-ANOMALIES
PADDOCK, RJ
ARENSMAN, RM
JOURNAL OF PEDIATRIC SURGERY, 1982, 17 (05) : 563 - 566