ASPARTYLGLUCOSAMINURIA IN THE UNITED-STATES

被引：0

作者：

HREIDARSSON, S

THOMAS, GH

VALLE, DL

STEVENSON, RE

TAYLOR, H

MCCARTY, J

COKER, SB

GREEN, WR

机构：

[1] JOHN F KENNEDY INST,707 N BROADWAY,BALTIMORE,MD 21205

[2] HOWARD HUGHES MED INST,DEPT PEDIAT,BALTIMORE,MD

[3] JOHNS HOPKINS UNIV,SCH MED,WILMER EYE INST,BALTIMORE,MD 21205

[4] JOHNS HOPKINS UNIV,SCH MED,DEPT PATHOL,BALTIMORE,MD 21205

[5] WALTER REED ARMY MED CTR,WASHINGTON,DC 20012

[6] GREENWOOD GENET CTR,GREENWOOD,SC 29646

来源：

CLINICAL GENETICS | 1983年 / 23卷 / 06期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：427 / 435

页数：9

共 25 条

[1] ASPARTYLGLUCOSAMINURIA .1. FINE-STRUCTURAL STUDIES ON LIVER, KIDNEY AND BRAIN [J].

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AUTIO, S ;

PALO, J ;

RIEKKINEN, P ;

HALTIA, M .

ACTA NEUROPATHOLOGICA, 1972, 20 (03) :207-+

[2]

AULA P, 1973, CLIN GENET, V4, P297

[3] ENZYMATIC DIAGNOSIS AND CARRIER DETECTION OF ASPARTYLGLUCOSAMINURIA USING BLOOD-SAMPLES [J].

AULA, P ;

RAIVIO, K ;

AUTIO, S .

PEDIATRIC RESEARCH, 1976, 10 (06) :625-629

[4]

AULA P, 1974, HUMANGENETIK, V25, P207

[5]

AUTIO S, 1974, Birth Defects Original Article Series, V10, P193

[6]

AUTIO S, 1973, ANN CLIN RES, V5, P149

[7]

AUTIO S, 1982, COMMUNICATION

[8]

Borud O, 1978, J Inherit Metab Dis, V1, P95, DOI 10.1007/BF01805680

[9]

Borud O, 1978, Monogr Hum Genet, V10, P23

[10]

GALEWICZ A, 1974, J MENT DEFIC RES, V18, P135

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