(Q95790079)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

30 May 2020

title

A new variant phenotype of the group-specific component (Gc) found in a Japanese family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

30 May 2020

Neues zur Genetik und Klassifikation der Muskeldystrophien (German)

1 reference

19 February 2023

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4676024

19 February 2023

1 reference

19 February 2023

author name string

K. Omoto

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4676024

19 February 2023

H. Cleve

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4676024

19 February 2023

S. Misawa

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4676024

19 February 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4676024

19 February 2023

publication date

1 September 1972

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

30 May 2020

http://link.springer.com/content/pdf/10.1007/BF01789595.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF01789595/fulltext.html

19 February 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF01789595

19 February 2023

1 reference

Japanese Journal of Human Genetics

19 February 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

30 May 2020

volume

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

30 May 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

30 May 2020

page(s)

1-9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

[A new x-chromosomal muscular dystrophy]

30 May 2020

cites work

4

1 reference

Duchenne's Muscular Dystrophy and the Xg Blood Groups: a Search for Linkage.

19 February 2023

7

1 reference

Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.

19 February 2023

8

1 reference

The sex ratio of mutation rates of sex-linked recessive genes in man with particular reference to Duchenne type muscular dystrophy

19 February 2023

10

1 reference

Survival in x-chromosomal muscular dystrophy

19 February 2023

13

1 reference

MUSCLE HISTOLOGY IN CARRIERS OF DUCHENNE MUSCULAR DYSTROPHY.

19 February 2023

16

1 reference

Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.

19 February 2023

17

1 reference

Abnormalities of the Electrocardiogram in Female Carriers of Duchenne Muscular Dystrophy

19 February 2023

18

1 reference

The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups

19 February 2023

20

1 reference

Mutation rate in Duchenne type of muscular dystrophy

19 February 2023

24

1 reference

Hereditary Myopathy Limited to Females

19 February 2023

26

1 reference

X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression

19 February 2023

33

1 reference

Benign sex-linked muscular dystrophy: Clinical and pathological features

19 February 2023

34

1 reference

[Simple recessive form of progressive muscular dystrophy with a genealogical chart from Emmental, Switzerland.]

19 February 2023

38

1 reference

Colour blindness and the Duchenne-type muscular dystrophy

19 February 2023

39

1 reference

CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. I. SERUM ENZYMES IN PROGRESSIVE MUSCULAR DYSTROPHY (TYPE I, II, IIIA)

19 February 2023

43

1 reference

CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE

19 February 2023

45

1 reference

Genetic studies of a family with two unusual autosomal dominant conditions: muscular dystrophy and Pelger-Huet anomaly. Clinical, pathologic and linkage considerations

19 February 2023

47

1 reference

Clinical, genetic and electrocardiographic studies in childhood muscular dystrophy

19 February 2023

49

1 reference

Muscular dystrophy in Northern Ireland. IV. Some additional data

19 February 2023

51

1 reference

X-linked scapuloperoneal syndrome

19 February 2023

54

1 reference

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

19 February 2023

56

1 reference

On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies

19 February 2023

57

1 reference

MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE

19 February 2023

59

1 reference

On the classification, natural history and treatment of the myopathies.

19 February 2023

61

1 reference

19 February 2023

Identifiers

DOI

10.1007/BF01789595

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4676024%20AND%20SRC:MED&resulttype=core&format=json

30 May 2020

1 reference