INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-2 WITH NORMAL LEVELS OF ISOCITRATE DEHYDROGENASE

被引：40

作者：

GLASS, IA

SWINDLEHURST, CA

AITKEN, DA

MCCREA, W

BOYD, E

机构：

[1] ROYAL HOSP SICK CHILDREN,DEPT CHILD HLTH,GLASGOW G3 8SJ,SCOTLAND

[2] ROYAL SCOTTISH NATL HOSP,LARBERT FK5 4EJ,STIRLING,SCOTLAND

来源：

JOURNAL OF MEDICAL GENETICS | 1989年 / 26卷 / 02期

关键词：

D O I：

10.1136/jmg.26.2.127

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：127 / 140

页数：14

共 10 条

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[2] INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 2 IN A MALFORMED INFANT WITH KARYOTYPE 46,XX,DEL(2)(Q31Q33) [J].

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[5]

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[6] PROBABLE ASSIGNMENT OF SOLUBLE ISOCITRATE DEHYDROGENASE (IDH1) TO 2Q33.3 [J].

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[7] IDENTICAL MULTIPLE CONGENITAL-ANOMALIES MENTAL-RETARDATION (MCA/MR) SYNDROME DUE TO DEL(2)(Q32) IN 2 SISTERS WITH INTRACHROMOSOMAL INSERTIONAL TRANSLOCATION IN THEIR FATHER [J].

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[8]

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[9]

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[10] DELETION 2Q - 2 NEW CASES WITH KARYOTYPES 46,XY,DEL(2)(Q31Q33) AND 46,XX,DEL(2)(Q36) [J].

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