MONOSOMY, TRISOMY, FRAGILE SITES, AND REARRANGEMENTS OF CHROMOSOME NO-1 IN A MENTALLY-RETARDED MALE WITH MULTIPLE CONGENITAL-ANOMALIES

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作者：

NEU, RL

KOUSSEFF, BG

MADAN, S

ESSIG, YP

MILLER, K

TEDESCO, TA

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CLINICAL GENETICS | 1988年 / 33卷 / 02期

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Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

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页码：73 / 77

页数：5

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[9] A FAMILIAL X-LINKED MENTAL-RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL-ANOMALIES, MEGALOGENITALIA AND A FRAGILE X-CHROMOSOME
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[10] DIRECT ANALYSIS OF THE FMR-1 GENE PROVIDES AN EXPLANATION FOR AN EXCEPTIONAL CASE OF A FRAGILE-X NEGATIVE, MENTALLY-RETARDED MALE IN A FRAGILE-X FAMILY
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