ACROCEPHALOSYNDACTYLIA ASSOCIATED WITH A CHROMOSOMAL TRANSLOCATION - 46,XX,T (2P- - CQ+)

被引：14

作者：

DODSON, WE

MUSELES, M

KENNEDY, JL

ALAISH, M

机构：

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1970年 / 120卷 / 04期

关键词：

D O I：

10.1001/archpedi.1970.02100090134019

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：360 / &

共 21 条

[1] A FAMILIAL 3/18 RECIPROCAL TRANSLOCATION RESULING IN CHROMOSOME DUPLICATION-DEFICIENCY (3+-18Q-)
AARSKOG, D
[J]. ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (04): : 397 - &
[2] HUMAN CHROMOSOME MORPHOLOGY .I. STUDIES ON NORMAL CHROMOSOME CHARACTERIZATION, CLASSIFICATION AND KARYOTYPING
ALAISH, MS
[J]. CANADIAN JOURNAL OF GENETICS AND CYTOLOGY, 1969, 11 (02): : 370 - +
[3] Apert E, 1906, B MEM SOC MED HOP P, V23
[4] Battaglino G, 1967, Fracastoro, V60, P243
[5] Beaudoing A, 1967, Pediatrie, V22, P723
[6] BLANK CE, 1960, ANN HUM GENET, V24, P151
[7] BROWN WMC, 1967, HUMAN POPULATION CYT, P23
[8] Caramia G, 1968, Clin Pediatr (Bologna), V50, P453
[9] FORD CE, 1960, AM J HUM GENET, V12, P104
[10] Frerichs C T, 1967, Nebr State Med J, V52, P491