NEW CHROMOSOMAL SYNDROME - MILLER-DIEKER SYNDROME AND MONOSOMY 17P13

被引:100
作者
STRATTON, RF
DOBYNS, WB
AIRHART, SD
LEDBETTER, DH
机构
[1] BAYLOR COLL MED,DEPT MED,KLEBERG CYTOGENET LAB,HOUSTON,TX 77030
[2] BAYLOR COLL MED,DEPT NEUROL,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
[4] TEXAS CHILDRENS HOSP,NEUROL SERV,HOUSTON,TX 77030
关键词
D O I
10.1007/BF00273000
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:193 / 200
页数:8
相关论文
共 31 条
[11]  
ERHARDT A, 1914, ALLG Z PSYCHIAT, V71, P656
[12]   LISSENCEPHALY (AGYRIA) SYNDROME IN SIBLINGS - COMPUTERIZED TOMOGRAPHIC AND NEUROPATHOLOGIC FINDINGS [J].
GARCIA, CA ;
DUNN, D ;
TREVOR, R .
ARCHIVES OF NEUROLOGY, 1978, 35 (09) :608-611
[13]   AGYRIA-PACHYGYRIA (LISSENCEPHALY SYNDROME) [J].
JELLINGER, K ;
RETT, A .
NEUROPADIATRIE, 1976, 7 (01) :66-91
[14]  
JONES KL, 1980, PEDIATRICS, V66, P277
[15]   THE ASSOCIATION OF THE DIGEORGE ANOMALAD WITH PARTIAL MONOSOMY OF CHROMOSOME 22 [J].
KELLEY, RI ;
ZACKAI, EH ;
EMANUEL, BS ;
KISTENMACHER, M ;
GREENBERG, F ;
PUNNETT, HH .
JOURNAL OF PEDIATRICS, 1982, 101 (02) :197-200
[16]  
LEDBETTER DH, 1982, AM J HUM GENET, V34, P278
[17]   DELETIONS OF CHROMOSOME-15 AS A CAUSE OF THE PRADER-WILLI SYNDROME [J].
LEDBETTER, DH ;
RICCARDI, VM ;
AIRHART, SD ;
STROBEL, RJ ;
KEENAN, BS ;
CRAWFORD, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (06) :325-329
[18]   MULTIGENE FAMILY FOR SARCOMERIC MYOSIN HEAVY-CHAIN IN MOUSE AND HUMAN DNA - LOCALIZATION ON A SINGLE CHROMOSOME [J].
LEINWAND, LA ;
FOURNIER, REK ;
NADALGINARD, B ;
SHOWS, TB .
SCIENCE, 1983, 221 (4612) :766-769
[19]   LISSENCEPHALY IN 2 SIBLINGS [J].
MILLER, JQ .
NEUROLOGY, 1963, 13 (10) :841-&
[20]  
MUENCHHOFF C, 1965, ACTA NEUROPATH BERL, V4, P469