(Q33672918)

English

Paternal and maternal transmission of pseudohypoparathyroidism type Ia in a family with Albright hereditary osteodystrophy: no evidence of genomic imprinting

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Paternal and maternal transmission of pseudohypoparathyroidism type Ia in a family with Albright hereditary osteodystrophy: no evidence of genomic imprinting (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Albright's hereditary osteodystrophy

1 reference

based on heuristic

inferred from title

author name string

Schuster V

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Kress W

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Kruse K

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 January 1994

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

31

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

84

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Pseudo-pseudohypoparathyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049615

21 June 2018

Imprinting in Albright's hereditary osteodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049615

21 June 2018

Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049615

21 June 2018

Albright's hereditary osteodystrophy and defective G proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049615

21 June 2018

Endocrine and molecular biological studies in a German family with Albright hereditary osteodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049615

30 October 2018

A simplified diagnostic test in hypoparathyroidism and pseudohypoparathyroidism type I with synthetic 1-38 fragment of human parathyroid hormone

1 reference

https://pubmed.ncbi.nlm.nih.gov/8151649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G protein Gs alpha (GNAS 1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8151649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughter

1 reference

https://pubmed.ncbi.nlm.nih.gov/8151649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8151649

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.31.1.84

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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