RING CHROMOSOME-22 KARYOTYPE IN A PATIENT WITH OPITZ (BBBG) SYNDROME

被引：12

作者：

CHRISTODOULOU, J ^{[1
]}

BANKIER, A ^{[1
]}

LOUGHNAN, P ^{[1
]}

机构：

[1] ROYAL CHILDRENS HOSP,DEPT NEONATOL,PARKVILLE,VIC 3052,AUSTRALIA

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 37卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320370324

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：422 / 424

页数：3

共 11 条

[1]

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[6] DOES RING SYNDROME EXIST - AN ANALYSIS OF 207 CASE-REPORTS ON PATIENTS WITH A RING AUTOSOME [J].

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[7]

OPITZ J M, 1969, Birth Defects Original Article Series, V5, P95

[8] 4 NEW CASES OF RING 21 AND 22 INCLUDING FAMILIAL TRANSMISSION OF RING 21 [J].

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[9] CONGENITAL ANAL ANOMALIES IN 2 FAMILIES WITH THE OPITZ-G SYNDROME [J].

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[10] BBBG SYNDROME OR OPITZ SYNDROME - NEW FAMILY [J].

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