A METHOD FOR PRENATAL DIAGNOSIS OF CONGENITAL HYPERURICEMIA

被引：17

作者：

BERMAN, PH

BALIS, ME

DANCIS, J

机构：

[1] Department of Psychiatry and Neurology, New York University School of Medicine, New York

[2] Department of Pediatrics, New York University School of Medicine, New York

[3] Sloan-Kettering Institute for Cancer Research, New York

来源：

JOURNAL OF PEDIATRICS | 1969年 / 75卷 / 03期

关键词：

D O I：

10.1016/S0022-3476(69)80279-9

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

[No abstract available]

引用

页码：488 / &

共 12 条

[1]

BERMAN PH, 1968, J LAB CLIN MED, V71, P247

[2] ANTEPARTUM DIAGNOSIS OF GENETIC DISEASES [J].

DANCIS, J .

JOURNAL OF PEDIATRICS, 1968, 72 (02) :301-+

[3]

FUJIMOTO WY, 1968, LANCET, V2, P511

[4] FAMILIAL DISORDER OF URIC ACID METABOLISM + CENTRAL NERVOUS SYSTEM FUNCTION [J].

LESCH, M ;

NYHAN, WL .

AMERICAN JOURNAL OF MEDICINE, 1964, 36 (04) :561-&

[5] CHROMATOGRAPHIC SEPARATION OF NUCLEOSIDE PHOSPHATES ON DIETHYLAMINOETHYLCELLULOSE PAPER [J].

MORRISON, JF .

ANALYTICAL BIOCHEMISTRY, 1968, 24 (01) :106-&

[6] PATTERNS OF ENZYME DEVELOPMENT UTILIZING CULTIVATED HUMAN FETAL CELLS DERIVED FROM AMNIOTIC FLUID [J].

NADLER, HL .

BIOCHEMICAL GENETICS, 1968, 2 (02) :119-+

[7] PRENATAL DETECTION OF GENETIC DEFECTS [J].

NADLER, HL .

JOURNAL OF PEDIATRICS, 1969, 74 (01) :132-+

[8]

NADLER HL, 1968, PEDIATRICS, V42, P912

[9] ENZYME DEFECT ASSOCIATED WITH A SEX-LINKED HUMAN NEUROLOGICAL DISORDER AND EXCESSIVE PURINE SYNTHESIS [J].

SEEGMILLER, JE ;

ROSENBLOOM, FM ;

KELLEY, WN .

SCIENCE, 1967, 155 (3770) :1682-+

[10]

SMITH I, 1960, CHROMATOGR ELECTROPH, V1, P234

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