TRISOMY-2Q

被引：6

作者：

DALLAPICCOLA, B

FORABOSCO, A

CALABRO, A

机构：

[1] UNIV ROME,DEPT MED GENET,I-00100 ROME,ITALY

[2] UNIV MODENA,DEPT HUMAN NORMAL ANAT,I-41100 MODENA,ITALY

来源：

ACTA GENETICAE MEDICAE ET GEMELLOLOGIAE | 1975年 / 24卷 / 3-4期

关键词：

D O I：

10.1017/S0001566000010424

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：307 / 310

页数：4

共 9 条

[1]

DAVISON B C C, 1970, Journal of Medical Genetics, V7, P81, DOI 10.1136/jmg.7.1.81

[2]

FITZGERA.MG, 1974, AUST PAEDIATR J, V10, P180

[3]

FORABOSCO A, 1973, ANN GENET-PARIS, V16, P255

[4] 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-&

[5]

LAURENT C, 1971, ANN GENET-PARIS, V14, P33

[6]

LISCO E, 1967, ANN GENET-PARIS, V10, P42

[7] AN UNUSUAL CHROMOSOME ABNORMALITY - 2/D TRANSLOCATION [J].

REISMAN, LE ;

KASAHARA, S .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 115 (05) :625-&

[8]

RICCI N, 1968, ANN GENET-PARIS, V11, P111

[9] PLACENTAL CHORANGIOMATA AND MENTAL DEFICIENCY IN A CHILD WITH 2/15 TRANSLOCATION - 46,XX,T(2Q- - 15Q+) [J].

WURSTER, DH ;

HOEFNAGEL, D ;

BENIRSCHKE, K ;

ALLEN, FH .

CYTOGENETICS, 1969, 8 (05) :389-+

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