(Q33585048)

28 July 2017

MUSCULAR DYSTROPHY (DUCHENNE) IN A GIRL WITH TURNER'S SYNDROME. (English)

1 reference

28 July 2017

1 reference

FERRIER P

1

1 reference

28 July 2017

BAMATTER F

series ordinal

2

1 reference

28 July 2017

KLEIN D

series ordinal

3

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 March 1965

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

2

1 reference

28 July 2017

38-46

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28 July 2017

1

1 reference

Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

GENETICS AND DISEASES OF MUSCLE.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

X-chromosome mosaicism in females with muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

Evidence that the Xg blood group genes are on the short arm of the X chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

Abnormalities of sex chromosome constitution in newborn babies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

Gene action in the X-chromosome of the mouse (Mus musculus L.)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

Congenital anomalies associated with gonadal aplasia; review of 55 cases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012803

[GONADAL DYSGENESIS (TURNER'S SYNDROME): A RARE DISEASE BUT VALUABLE INSTRUCTIVELY; A CHROMOSOME STUDY OF 35 CASES.]

31 October 2018

1 reference

12 December 2020

Abnormal sexual development associated with sex chromosome mosaicism. Report of three cases

1 reference

12 December 2020

Colour blindness and the Duchenne-type muscular dystrophy

1 reference

12 December 2020

THE PATHOLOGY AND CYTOGENETICS OF GONADAL AGENESIS

1 reference

12 December 2020

THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS

1 reference

12 December 2020

INCIDENCE OF TURNER'S SYNDROME IN JAPANESE DWARFED GIRLS

1 reference

12 December 2020

Cytogenetic studies in primary amenorrhoea

1 reference

12 December 2020

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

1 reference

12 December 2020

The Carpal Sign in Gonadal Dysgenesis

1 reference

12 December 2020

Muscular dystrophy in Northern Ireland, I. An account of the condition in fifty-one families

1 reference

12 December 2020

Serum Enzymes in Carriers of Muscular Dystrophy

1 reference

12 December 2020

Autosomal recessive inheritance of Duchennetype muscular dystrophy

1 reference

12 December 2020

Progressive muscular dystrophy: autosomal recessive type

1 reference

12 December 2020

Identifiers

PMCID

1012803

1 reference

28 July 2017

1 reference