DELETION 2Q - 2 NEW CASES WITH KARYOTYPES 46,XY,DEL(2)(Q31Q33) AND 46,XX,DEL(2)(Q36)

被引：56

作者：

YOUNG, RS ^{[1
]}

SHAPIRO, SD ^{[1
]}

HANSEN, KL ^{[1
]}

HINE, LK ^{[1
]}

RAINOSEK, DE ^{[1
]}

GUERRA, FA ^{[1
]}

机构：

[1] SANTA ROSA MED CTR,SAN ANTONIO,TX

来源：

JOURNAL OF MEDICAL GENETICS | 1983年 / 20卷 / 03期

关键词：

D O I：

10.1136/jmg.20.3.199

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：199 / 202

页数：4

共 6 条

[1]

ANTICH J, 1981, CLIN GENET, V19, P489

[2] INTERSTITIAL DELETION OF LONG ARM OF CHROMOSOME 2 IN A POLYMALFORMED NEWBORN-KARYOTYPE - 46,XX,DEL(2)(Q21-Q24) [J].

FRYNS, JP ;

VANBOSSTRAETEN, B ;

MALBRAIN, H ;

VANDENBERGHE, H .

HUMAN GENETICS, 1977, 39 (02) :233-238

[3] AUTOSOMAL TRANSLOCATION IN A MENTALLY RETARDED MALE CHILD WITH 46,XY,T(2Q-13Q+) COMPLEMENT - CASE REPORT AND REVIEW [J].

GENEST, P ;

LACHANCE, R ;

POTY, J ;

JACOB, D .

JOURNAL OF MEDICAL GENETICS, 1971, 8 (04) :504-&

[4] PARTIAL DELETION OF CHROMOSOME-2 MIMICKING A PHENOTYPE OF TRISOMY-18 - CASE-REPORT WITH AUTOPSY [J].

MCCONNELL, TS ;

KORNFELD, M ;

MCCLELLAN, G ;

AASE, J .

HUMAN PATHOLOGY, 1980, 11 (02) :202-205

[5]

TAYSI K, 1981, ANN GENET-PARIS, V24, P245

[6] GIRL WITH A DELETION (2)(Q34Q36) - CYTOGENETIC AND CLINICAL OBSERVATIONS [J].

WARTER, S ;

LAUSECKER, C ;

PENNERATH, A .

HUMAN GENETICS, 1976, 32 (02) :225-227

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