HIRSCHSPRUNGS-DISEASE, DISTINCTIVE FACIES, AND MICROCEPHALY

被引:5
作者
BANKIER, A
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D O I
10.1136/jmg.26.4.287
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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页码:287 / 288
页数:2
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共 12 条
[1]  
BRANSKI D, 1979, PEDIATRICS, V63, P803
[2]  
Brunoni D, 1983, J Clin Dysmorphol, V1, P20
[3]  
CURRY C J R, 1987, American Journal of Medical Genetics, V26, P45, DOI 10.1002/ajmg.1320260110
[4]  
GOLDBERG RB, 1981, J CRAN GENET DEV BIO, V1, P185
[5]   UNKNOWN SYNDROME - HIRSCHSPRUNGS-DISEASE, MICROCEPHALY, AND IRIS COLOBOMA - A NEW SYNDROME OF DEFECTIVE NEURONAL MIGRATION [J].
HURST, JA ;
MARKIEWICZ, M ;
KUMAR, D ;
BRETT, EM .
JOURNAL OF MEDICAL GENETICS, 1988, 25 (07) :494-497
[6]   HIRSCHSPRUNGS DISEASE ASSOCIATED WITH CONGENITAL HEART MALFORMATION, BROAD BIG TOES, AND ULNAR POLYDACTYLY IN SIBS - CASE FOR FETOSCOPY [J].
LAURENCE, KM ;
PROSSER, R ;
ROCKER, I ;
PEARSON, JF ;
RICHARDS, C .
JOURNAL OF MEDICAL GENETICS, 1975, 12 (04) :334-338
[7]  
REYNOLDS JF, 1983, PEDIATRICS, V71, P246
[8]   HIRSCHSPRUNG DISEASE ASSOCIATED WITH POLYDACTYLY, UNILATERAL RENAL AGENESIS, HYPERTELORISM, AND CONGENITAL DEAFNESS - A NEW AUTOSOMAL RECESSIVE SYNDROME [J].
SANTOS, H ;
MATEUS, J ;
LEAL, MJ .
JOURNAL OF MEDICAL GENETICS, 1988, 25 (03) :204-205
[9]  
TORIELLO HV, 1988, DYSMORPHOL CLIN GENE, V1, P155
[10]   CONCURRENT DENOVO INTERSTITIAL DELETION OF BAND 2P22 AND RECIPROCAL TRANSLOCATION (3-7)(P21-Q22) [J].
WEBB, GC ;
KEITH, CG ;
CAMPBELL, NT .
JOURNAL OF MEDICAL GENETICS, 1988, 25 (02) :125-127