STUDIES OF MALFORMATION SYNDROMES OF MAN .47. DISAPPEARANCE OF SPERMATOGONIA IN FANCONI ANEMIA SYNDROME

被引：23

作者：

BARGMAN, GJ

SHAHIDI, NT

GILBERT, EF

OPITZ, JM

机构：

[1] UNIV WISCONSIN,CTR HLTH SCI,SCH MED,DEPT PEDIAT,MADISON,WI 53706

[2] UNIV WISCONSIN,CTR HLTH SCI,SCH MED,DEPT PATHOL,MADISON,WI 53706

[3] UNIV WISCONSIN,CTR HLTH SCI,SCH MED,DEPT MED GENET,WISCONSIN CLIN GENET CTR,MADISON,WI 53706

来源：

关键词：

D O I：

10.1007/BF00480592

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：163 / 168

页数：6

共 18 条

COWDELL, RH ;

PHIZACKERLEY, PJR ;

PYKE, DA .

[2]

Cussen L J, 1965, Med J Aust, V2, P367

[3]

DELCASTILLO EB, 1947, J CLIN ENDOCRINOL, V7, P493

[4]

DUNN HG, 1964, CAN MED ASSOC J, V91, P1106

[5]

Fanconi, 1927, JB KINDERHEILK, V117, P257

[6]

GERMAN J, 1969, AM J HUM GENET, V21, P196

[7]

GERMAN J, 1969, Birth Defects Original Article Series, V5, P117

[8]

GMYREK D, 1964, Z Kinderheilkd, V91, P297, DOI 10.1007/BF00439778

[9]

GONZALEZ CH, 1976, BIRTH DEFECTS OAS

[10]

MEISNER LF, 1976, 1976 P INT S APL AN