MULTIPLE SKELETAL ANOMALIES IN 13Q- SYNDROME

被引：7

作者：

CHEMKE, J

FISHEL, E

ZALISH, M

SAGIV, M

机构：

[1] KAPLAN HOSP,DEPT ROENTGEN,REHOVOTH,ISRAEL

[2] KAPLAN HOSP,DEPT OPHTHALMOL,REHOVOTH,ISRAEL

[3] KAPLAN HOSP,DEPT PATHOL,REHOVOTH,ISRAEL

来源：

EUROPEAN JOURNAL OF PEDIATRICS | 1978年 / 128卷 / 01期

关键词：

D O I：

10.1007/BF00496923

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：27 / 31

页数：5

共 9 条

[1]

ALLDERDICE PW, 1969, AM J HUM GENET, V21, P499

[2] PARTIAL DELETION OF LONG ARM OF CHROMOSOME NO 13 [J].

CUSCHIERI, A ;

AGIUS, PV ;

SCHERES, JMJC .

HUMAN GENETICS, 1977, 36 (03) :341-344

[3] 13Q- DELETION SYNDROME [J].

GRACE, E ;

DRENNAN, J ;

COLVER, D ;

GORDON, RR .

JOURNAL OF MEDICAL GENETICS, 1971, 8 (03) :351-&

[4] CHROMOSOMAL DELETION AND RETINOBLASTOMA [J].

KNUDSON, AG ;

MEADOWS, AT ;

NICHOLS, WW ;

HILL, R .

NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (20) :1120-1123

[5] CHROMOSOME PREPARATIONS OF LEUKOCYTES CULTURED FROM HUMAN PERIPHERAL BLOOD [J].

MOORHEAD, PS ;

NOWELL, PC ;

MELLMAN, WJ ;

BATTIPS, DM ;

HUNGERFORD, DA .

EXPERIMENTAL CELL RESEARCH, 1960, 20 (03) :613-616

[6]

NOEL B, 1976, CLIN GENET, V9, P593

[7]

ORYE E, 1974, CLIN GENET, V5, P457

[8]

SEABRIGH.M, 1971, LANCET, V2, P971

[9]

WILSON MG, 1973, AM J HUM GENET, V25, P57

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