(Q35571081)

English

Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype

scientific article published on August 1999

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10465110%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10465110%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

Richard C Trembath

5

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12 December 2019

author name string

Bijlsma EK

1

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12 December 2019

Aalfs CM

2

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12 December 2019

Sluitjer S

3

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12 December 2019

Oude Luttikhuis ME

4

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12 December 2019

Hoovers JM

6

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12 December 2019

Hennekam RC

7

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12 December 2019

language of work or name

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publication date

1 August 1999

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12 December 2019

Journal of Medical Genetics

1 reference

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12 December 2019

36

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12 December 2019

604-609

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12 December 2019

8

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12 December 2019

RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762967

12 July 2018

A high-resolution cytogenetic map of human chromosome 2: localization of 434 cosmid markers by direct R-banding fluorescence in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762967

12 July 2018

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762967

12 July 2018

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=1762967

12 July 2018

Sequence organization of the human chromosome 2q telomere.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762967

12 July 2018

Defect of Receptor–Cyclase Coupling Protein in Pseudohypoparathyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1762967

12 July 2018

Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/10465110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Double synchronization of human lymphocyte cultures: selection for high-resolution banded metaphases in the first and second division

1 reference

https://pubmed.ncbi.nlm.nih.gov/10465110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered

1 reference

https://pubmed.ncbi.nlm.nih.gov/10465110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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12 December 2019

1 reference

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12 December 2019

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