A NEW SYNDROME OF PROXIMAL DELETION OF THE LONG ARM OF CHROMOSOME-1 - 1Q21-23-]1Q25

被引：36

作者：

TAYSI, K ^{[1
]}

SEKHON, GS ^{[1
]}

HILLMAN, RE ^{[1
]}

机构：

[1] MILWAUKEE CHILDRENS HOSP,MILWAUKEE,WI 53233

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1982年 / 13卷 / 04期

关键词：

D O I：

10.1002/ajmg.1320130411

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：423 / 430

页数：8

共 10 条

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[4]

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[5] PRIMARY HYPOTHYROIDISM, GROWTH-HORMONE DEFICIENCY AND CONGENITAL-MALFORMATIONS IN A CHILD WITH KARYOTYPE 46,XY,DEL(1)(Q25Q32) [J].

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[6]

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[7]

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[8] PARTIAL DELETION OF 1Q, FOLLOWING A PERICENTRIC INVERSION, IN A BOY WITH MULTIPLE MINOR MORPHOLOGIC ANOMALIES AND MENTAL-RETARDATION [J].

SCHWANITZ, G ;

SCHMID, P ;

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GROSSE, KP .

ACTA GENETICAE MEDICAE ET GEMELLOLOGIAE, 1977, 26 (02) :173-175

[9] DELETION IN LONG ARM OF CHROMOSOME-1 FROM A SUBJECT WITH MULTIPLE CONGENITAL ANOMALIES - REPOSITORY IDENTIFICATION NO GM-2025 [J].

SEKHON, GS ;

HILLMAN, RE ;

YU, R ;

ARONSON, MM ;

GREENE, AE ;

CORIELL, LL .

CYTOGENETICS AND CELL GENETICS, 1978, 21 (03) :176-176

[10]

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