APPARENT G-MONOSOMY, G-DELETION, AND INCOMPLETE DOWNS-SYNDROME IN A SINGLE FAMILY

被引：15

作者：

SCHMIDT, R

MUNDEL, G

ROSENBLATT, M

KATZNELSON, MB

机构：

[1] ASAF HAROFE GOVT HOSP, CYTOGENET LAB, ZRIFIN, ISRAEL

[2] ASAF HAROFE GOVT HOSP, PEDIAT DEPT C, ZRIFN, ISRAEL

[3] TEL HASHOMER GOVT HOSP, CYTOGENET INST, DEPT HUMAN GENET, TEL AVIV, ISRAEL

[4] TEL AVIV UNIV, SCH MED, TEL AVIV, ISRAEL

来源：

JOURNAL OF MEDICAL GENETICS | 1972年 / 9卷 / 04期

关键词：

D O I：

10.1136/jmg.9.4.457

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：457 / 461

页数：5

共 18 条

[1] AUTOSOMAL MONOSOMY IN MAN - COMPLETE MONOSOMY G (21-22) IN A 4-AND-1/2-YEAR-OLD MENTALLY RETARDED GIRL [J].

ALAISH, MS ;

DELACRUZ, F ;

GOLDSMITH, LA ;

VOLPE, J ;

MELLA, G ;

ROBINSON, JC .

NEW ENGLAND JOURNAL OF MEDICINE, 1967, 277 (15) :777-+

[2]

BAUCHINGER M, 1968, HUMANGENETIK, V6, P303

[3]

BLANK C E, 1969, Journal of Medical Genetics, V6, P220, DOI 10.1136/jmg.6.2.220

[4]

Broyer M, 1966, Presse Med, V74, P791

[5] MONOSOMY FOR A G AUTOSOME [J].

CHALLACOMBE, DN ;

TAYLOR, A .

ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (233) :113-+

[6]

Cummins H., 1936, ANAT REC, V64, P11

[7] A CHILD WITH A GROUP-G RING CHROMOSOME [J].

HOEFNAGEL, D ;

SCHROEDE.M ;

BENIRSCH. .

HUMANGENETIK, 1967, 4 (01) :52-52

[8]

LEJEUNE J, 1964, CR HEBD ACAD SCI, V259, P4187

[9]

PENROSE LS, 1966, LANCET, V1, P497

[10] DERMATOGLYPHIC NOMOGRAM FOR DIAGNOSIS OF DOWNS SYNDROME [J].

REED, TE ;

BORGAONKAR, DS ;

CONNEALLY, PM ;

YU, PL ;

NANCE, WE ;

CHRISTIAN, JC .

JOURNAL OF PEDIATRICS, 1970, 77 (06) :1024-+

← 1 2 →