LINKAGE STUDIES IN AUTOSOMAL DOMINANT FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

被引：15

作者：

PADBERG, G

ERIKSSON, AW

VOLKERS, WS

BERNINI, L

VANLOGHEM, E

KHAN, PM

NIJENHUIS, LE

PRONK, JC

SCHREUDER, GMT

机构：

[1] LEIDEN STATE UNIV,DEPT NEUROL,2312 AV LEIDEN,NETHERLANDS

[2] LEIDEN STATE UNIV,DEPT HUMAN GENET,2312 AV LEIDEN,NETHERLANDS

[3] LEIDEN STATE UNIV,DEPT IMMUNOHAEMATOL,2312 AV LEIDEN,NETHERLANDS

[4] FREE UNIV AMSTERDAM,INST HUMAN GENET,1007 MC AMSTERDAM,NETHERLANDS

[5] DUTCH RED CROSS BLOOD TRANSFUS SERV,CENT LAB,AMSTERDAM,NETHERLANDS

来源：

JOURNAL OF THE NEUROLOGICAL SCIENCES | 1984年 / 65卷 / 03期

关键词：

D O I：

10.1016/0022-510X(84)90090-X

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：261 / 268

页数：8

共 14 条

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[3]

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[4] FAMILY STUDIES ON NUCLEOSIDE PHOSPHORYLASE AND THE SHORT ARM OF CHROMOSOME-14 [J].

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ROBSON, EB ;

ROGERS, PA ;

NOADES, JE ;

BUCKTON, KE ;

WATSON, AR .

ANNALS OF HUMAN GENETICS, 1981, 45 (JUL) :253-260

[5] GENES FOR IMMUNOGLOBULIN HEAVY-CHAINS AND FOR ALPHA-1-ANTITRYPSIN ARE LOCALIZED TO SPECIFIC REGIONS OF CHROMOSOME-14Q [J].

COX, DW ;

MARKOVIC, VD ;

TESHIMA, IE .

NATURE, 1982, 297 (5865) :428-431

[6]

Dystrophia musculorum progressiva, 1954, J AMER MED ASSOC, V154, DOI [10.1001/jama.1954.02940490080030, DOI 10.1001/JAMA.1954.02940490080030]

[7]

GEDDEDAHL T, 1981, ANN HUM GENET, V45, P143

[8]

HARNDEN DG, 1981, BIRTH DEFECTS ORIGIN, V17

[9]

HULTEN M, 1974, HEREDITAS, V76, P55

[10]

OTT J, 1974, AM J HUM GENET, V26, P588

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