NEW CASE OF TRISOMY FOR DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9-13)(P21-Q21)

被引：46

作者：

JOTTERAND, M ^{[1
]}

JUILLARD, E ^{[1
]}

机构：

[1] UNIV VAUDOIS, DIV GENET MED CTR HOSP, LAUSANNE, SWITZERLAND

来源：

HUMAN GENETICS | 1976年 / 33卷 / 03期

关键词：

D O I：

10.1007/BF00286845

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

收藏

页码：213 / 222

页数：10

相关论文

共 20 条

[1] BLOOM GE, 1968, AM J HUM GENET, V20, P495
[2] AN INHERITED CHROMOSOME ABERRATION IN A GIRL WITH SIGNS OF DE LANGE SYNDROME
BROHOLM, KA
EEGOLOFS.O
HALL, B
[J]. ACTA PAEDIATRICA SCANDINAVICA, 1968, 57 (06): : 547 - &
[3] TRISOMY FOR DISTAL SEGMENT OF CHROMOSOME-13 - NEW SYNDROME
ESCOBAR, JI
SANCHEZ, O
YUNIS, JJ
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1974, 128 (02): : 217 - 220
[4] PERICENTRIC INVERSION OF CHROMOSOME NO 13 IN A LARGE FAMILY LEADING TO DUPLICATION DEFICIENCY CAUSING CONGENITAL MALFORMATIONS IN 3 INDIVIDUALS
HAUKSDOTTIR, H
HALLDORSSON, S
JENSSON, O
MIKKELSEN, M
MCDERMOTT, A
[J]. JOURNAL OF MEDICAL GENETICS, 1972, 9 (04) : 413 - 421
[5] NUCLEAR ABNORMALITIES OF NEUTROPHILS IN D1 TRISOMY SYNDROME
HECHT, F
OLIVER, TK
HUEHNS, ER
LUTZNER, M
[J]. JOURNAL OF PEDIATRICS, 1964, 65 (6P2) : 1089 - +
[6] DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN CHROMOSOMAL TRIPLICATION - D1 TRISOMY SYNDROME
HUEHNS, ER
HECHT, F
KEIL, JV
MOTULSKY, AG
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1964, 51 (01) : 89 - &
[7] HUEHNS ER, 1964, LANCET, V1, P589
[8] MACINTYRE MN, 1964, AM SOC HUM GENET, V21
[9] CHROMOSOME PREPARATIONS OF LEUKOCYTES CULTURED FROM HUMAN PERIPHERAL BLOOD
MOORHEAD, PS
NOWELL, PC
MELLMAN, WJ
BATTIPS, DM
HUNGERFORD, DA
[J]. EXPERIMENTAL CELL RESEARCH, 1960, 20 (03) : 613 - 616
[10] IONOSPHERIC WINDS AND VISCOUS DISSIPATION
ROSENBERG, NW
ZIMMERMAN, SP
[J]. RADIO SCIENCE, 1972, 7 (03) : 377 - +