X-LINKED MUSCULAR-DYSTROPHY - PHENOTYPIC GENOTYPIC CORRELATION

被引：0

作者：

GUARD, E

ROADLEY, G

WATT, A

MUELLER, RF

机构：

[1] UNIV OTAGO,SCH MED,DEPT PAEDIAT,DUNEDIN,NEW ZEALAND

[2] DUNEDIN PUBL HOSP,DUNEDIN,NEW ZEALAND

来源：

NEW ZEALAND MEDICAL JOURNAL | 1992年 / 105卷 / 939期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：319 / 319

页数：1

共 7 条

[1]

BEGGS AH, 1990, HUM GENET, V86, P45

[2]

EMERY AEH, 1987, OXFORD MONOGRAPHS ME, V15

[3] ANALYSIS OF MOLECULAR DELETIONS WITH CDNA PROBES IN PATIENTS WITH DUCHENNE AND BECKER MUSCULAR-DYSTROPHIES [J].

GILGENKRANTZ, H ;

CHELLY, J ;

LAMBERT, M ;

RECAN, D ;

BARBOT, JC ;

VANOMMEN, GJB ;

KAPLAN, JC .

GENOMICS, 1989, 5 (03) :574-580

[4]

KOENIG M, 1989, AM J HUM GENET, V45, P498

[5] COMPLETE CLONING OF THE DUCHENNE MUSCULAR-DYSTROPHY (DMD) CDNA AND PRELIMINARY GENOMIC ORGANIZATION OF THE DMD GENE IN NORMAL AND AFFECTED INDIVIDUALS [J].

KOENIG, M ;

HOFFMAN, EP ;

BERTELSON, CJ ;

MONACO, AP ;

FEENER, C ;

KUNKEL, LM .

CELL, 1987, 50 (03) :509-517

[6]

MALHOTRA SB, 1988, SCIENCE, V242, P756

[7] An Explanation for the Phenotypic Differences between Patients Bearing Partial Deletions of the DMD Locus [J].

Monaco, Anthony P. ;

Bertelson, Corlee J. ;

Liechti-Gallati, Sabina ;

Moser, Hans ;

Kunkel, Louis M. .

GENOMICS, 1988, 2 (01) :90-95

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