(Q56969142)

14

object named as

M. Pericak-Vance

0 references

author name string

B. Weiffenbach

1

0 references

J. Dubois

2

0 references

D. Storvick

3

0 references

R. Tawil

4

0 references

S.J. Jacobsen

5

0 references

J. Gilbert

6

0 references

J.R. Mendell

8

0 references

S. Winokur

9

0 references

M.R. Altherr

10

0 references

P. Schultz

11

0 references

S. Olandt

12

0 references

R.R. Frants

13

0 references

R.C. Griggs

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

15

0 references

language of work or name

English

0 references

publication date

June 1993

0 references

published in

Nature Genetics

0 references

volume

4

0 references

issue

2

0 references

page(s)

165-169

0 references

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

STUDIES IN DISORDERS OF MUSCLE. II. CLINICAL MANIFESTATIONS AND INHERITANCE OF FACIOSCAPULOHUMERAL DYSTROPHY IN A LARGE FAMILY

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

A genetic linkage map of the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

Germline mosaicism and Duchenne muscular dystrophy mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

Germinal mosaicism in Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

High resolution gene mapping of the human alpha globin locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

A VNTR isolated by size selection of human DNA fragments detects RFLPs at the extremity of 1p and 4q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

Electrophoretic separations of large DNA molecules by periodic inversion of the electric field

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-165

7 January 2021