ACROCALLOSAL SYNDROME - ADDITIONAL MANIFESTATIONS

被引：27
作者：
CASAMASSIMA, AC
BENECK, D
GEWITZ, MH
HOROWITZ, MA
WOOLF, PK
PETTERSEN, IM
SHAPIRO, LR
机构：
[1] NEW YORK MED COLL,DEPT PEDIAT,VALHALLA,NY 10595
[2] NEW YORK MED COLL,DEPT PATHOL,VALHALLA,NY 10595
[3] NEW YORK MED COLL,DEPT OPHTHALMOL,VALHALLA,NY 10595
[4] LETCHWORTH DEV SERV,REG MED GENET SERV & LAB,THIELLS,NY
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 32卷 / 03期
关键词：
D O I：
10.1002/ajmg.1320320306
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：311 / 317
页数：7
相关论文
共 21 条
[11]  
SCHINZEL A, 1979, HELV PAEDIATR ACTA, V34, P141
[12]   HALLUX DUPLICATION, POSTAXIAL POLYDACTYLY, ABSENCE OF THE CORPUS-CALLOSUM, SEVERE MENTAL-RETARDATION, AND ADDITIONAL ANOMALIES IN 2 UNRELATED PATIENTS - A NEW SYNDROME [J].
SCHINZEL, A ;
SCHMID, W .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1980, 6 (03) :241-249
[13]  
SCHINZEL A, 1982, HUM GENET, V62, P382, DOI 10.1007/BF00304564
[14]  
SCHINZEL A, 1986, CLIN GENET, V30, P399
[15]   ACROCALLOSAL SYNDROME [J].
SCHINZEL, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 12 (02) :201-203
[16]  
SCHINZEL A, 1986, DW SMITH WORKSHOP MA
[17]  
SMITH D, 1982, RECOGNIZABLE PATTERS, P78
[18]  
TEMTAMY S, 1978, BIRTH DEFECTS-ORIG, V14, P426
[19]   HYPOGENITALISM IN THE ACROCALLOSAL SYNDROME [J].
TEMTAMY, SA ;
MEGUID, NA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1989, 32 (03) :301-305
[20]  
Toriello H V, 1986, Am J Med Genet Suppl, V2, P89
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