GENETICS AND DISEASES OF MUSCLE

被引：19

作者：

BOYER, SH

FAINER, DC

机构：

来源：

AMERICAN JOURNAL OF MEDICINE | 1963年 / 35卷 / 05期

关键词：

D O I：

10.1016/0002-9343(63)90134-7

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：622 / +

页数：1

共 89 条

[31]

FAINER DC, TO BE PUBLISHED

[32]

FITZGERALD PH, 1962, LANCET, V2, P456

[33]

GAMSTORP I, 1956, ACTA PAEDIATR STOC S, V108, P1

[34] Hereditary analysis in paroxysmal paralysis - II Announcement [J].

Gaupp, R ;

Kalden, O .

ZEITSCHRIFT FUR DIE GESAMTE NEUROLOGIE UND PSYCHIATRIE, 1942, 174 (02) :194-212

[35] CHEMICAL STUDIES OF SEVERAL VARIETIES OF HB M [J].

GERALD, PS ;

EFRON, ML .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1961, 47 (11) :1758-+

[36]

HED R, 1955, ACTA MED SCANDI S303, V151, P1

[37] CORRESPONDENCE BETWEEN GENETIC DATA AND POSITION OF AMINO ACID ALTERATION IN A PROTEIN [J].

HELINSKI, DR ;

YANOFSKY, C .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1962, 48 (02) :173-&

[38] SERUM ENZYMES IN CARRIERS OF MUSCULAR DYSTROPHY [J].

HUGHES, BP .

BRITISH MEDICAL JOURNAL, 1962, (5310) :963-&

[39] ALLELOMORPHISM AND THE CHEMICAL DIFFERENCES OF THE HUMAN HAEMOGLOBINS-A, HAEMOGLOBINS-S AND HAEMOGLOBINS-C [J].

HUNT, JA ;

INGRAM, VM .

NATURE, 1958, 181 (4615) :1062-1063

[40]

JACKSON CE, 1961, PEDIATRICS, V28, P77

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