PERSISTENT MILD HYPERPHENYLALANINEMIA IN VARIOUS ETHNIC GROUPS IN ISRAEL

被引：26

作者：

SZEINBERG, A

COHEN, BE

GOLAN, R

PELED, I

LAVI, U

CRISPIN, M

机构：

[1] departments of chemical pathology, Government Hospital Tel-Hashomer and Tel-Aviv University Medical School, Tel-Hashomer

[2] departments of chemical pediatrics, Government Hospital Tel-Hashomer and Tel-Aviv University Medical School, Tel-Hashomer

来源：

AMERICAN JOURNAL OF DISEASES OF CHILDREN | 1969年 / 118卷 / 04期

关键词：

D O I：

10.1001/archpedi.1969.02100040561003

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

[No abstract available]

引用

页码：559 / +

页数：1

共 25 条

[1]

BERMAN JL, 1968, PEDIATR RES, V2, P404

[2]

CARPENTER GG, 1968, PEDIATR CLIN N AM, V15, P313

[3]

COHEN B, TO BE PUBLISHED

[4]

COHEN BE, 1966, ISRAEL J MED SCI, V2, P156

[5]

COHEN BE, 1968, 1 P C INT ASS SCIENT, P794

[6]

GUTHRIE R, 1963, PEDIATRICS, V32, P338

[7] HYPERPHENYLALANEMIA [J].

HSIA, DYY ;

OFLYNN, ME .

METABOLISM-CLINICAL AND EXPERIMENTAL, 1967, 16 (02) :99-&

[8]

HSIA DYY, 1960, AM J HUM GENET, V12, P277

[9] DETECTION OF HETEROZYGOTES FOR PHENYLKETONURIA [J].

JERVIS, GA .

CLINICA CHIMICA ACTA, 1960, 5 (04) :471-476

[10]

JERVIS GA, 1967, AMINO ACID METABOLIS, P5

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