REPORT OF THE COMMITTEE ON CLINICAL DISORDERS, CHROMOSOME-ABERRATIONS AND UNIPARENTAL DISOMY

被引：61
作者：
FREZAL, J [1 ]
SCHINZEL, A [1 ]
机构：
[1] INST MED GENET, CH-8001 ZURICH, SWITZERLAND
来源：
CYTOGENETICS AND CELL GENETICS | 1991年 / 58卷 / 3-4期
关键词：
D O I：
10.1159/000133716
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
引用
收藏
页码：986 / 1052
页数：67
相关论文
共 548 条
[1]  
ALITALO T, 1991, AM J HUM GENET, V48, P31
[2]   ALAGILLE SYNDROME AND DELETION OF 20P [J].
ANAD, F ;
BURN, J ;
MATTHEWS, D ;
CROSS, I ;
DAVISON, BCC ;
MUELLER, R ;
SANDS, M ;
LILLINGTON, DM ;
EASTHAM, E .
JOURNAL OF MEDICAL GENETICS, 1990, 27 (12) :729-737
[3]  
[Anonymous], AM J MED GENET
[4]  
ANVRET M, 1991, HUM GENET, V86, P481
[5]  
ARCHIDIACONO N, 1991, HUM GENET, V86, P604
[6]  
ARIAS S, 1989, CYTOGENET CELL GENET, V51, P953
[7]   RECOMBINATIONS BETWEEN ALU REPEAT SEQUENCES THAT RESULT IN PARTIAL DELETIONS WITHIN THE C1-INHIBITOR GENE [J].
ARIGA, T ;
CARTER, PE ;
DAVIS, AE .
GENOMICS, 1990, 8 (04) :607-613
[8]   MUTATION OF THE SIGNAL PEPTIDE-ENCODING REGION OF THE PREPROPARATHYROID HORMONE GENE IN FAMILIAL ISOLATED HYPOPARATHYROIDISM [J].
ARNOLD, A ;
HORST, SA ;
GARDELLA, TJ ;
BABA, H ;
LEVINE, MA ;
KRONENBERG, HM .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) :1084-1087
[9]  
ARVEILER B, 1990, AM J HUM GENET, V46, P906
[10]   LINKAGE ANALYSIS SUGGESTS AT LEAST 2 LOCI FOR X-LINKED NON-SPECIFIC MENTAL-RETARDATION [J].
ARVEILER, B ;
ALEMBIK, Y ;
HANAUER, A ;
JACOBS, P ;
TRANEBJAERG, L ;
MIKKELSEN, M ;
PUISSANT, H ;
PIET, LL ;
MANDEL, JL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2) :473-483
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