DETECTION OF KLINEFELTERS-SYNDROME AT BIRTH

被引：7

作者：

HARRIS, JS

HELLER, RH

机构：

[1] SINAI HOSP, DEPT OBSTET & GYNECOL, BALTIMORE, MD USA

[2] SINAI HOSP, DEPT PEDIAT, BALTIMORE, MD USA

来源：

CLINICAL PEDIATRICS | 1974年 / 13卷 / 07期

关键词：

D O I：

10.1177/000992287401300705

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：581 / 587

页数：7

共 15 条

[1]

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[2] XXY (KLINEFELTERS) SYNDROME IN CHILDHOOD - DETECTION AND TREATMENT [J].

CALDWELL, PD ;

SMITH, DW .

JOURNAL OF PEDIATRICS, 1972, 80 (02) :250-+

[3]

CULLING CFA, 1966, SEX CHROMATIN

[4]

FERGUSONSMITH MA, 1959, LANCET, V1, P219

[5]

FERGUSONSMITH MA, 1958, LANCET, V1, P928

[6]

FROLAND A, 1969, DAN MED BULL, V16, P5

[7] X CHROMOSOME ABNORMALITIES AND OBSTETRICIAN - VALUE OF ROUTINE NUCLEAR SEXING OF NEWBORN INFANTS [J].

HARRIS, JS ;

ROBINSON, A .

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1971, 109 (04) :574-+

[8]

HOLMES LB, 1972, MENTAL RETARDATION A

[9] Syndrome characterized by gynecomastisa, aspermatogenesis without a-leydigism, and increased excietion of follicle-stimulating hormone [J].

Klinefelter, HF ;

Reifenstein, EC ;

Albright, F .

JOURNAL OF CLINICAL ENDOCRINOLOGY, 1942, 2 (11) :615-627

[10]

KLINGER H. P., 1957, ACTA ANAT, V30, P371

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