(Q34385428)

1 August 2017

Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3. (English)

1 reference

congenital dyserythropoietic anemia type I

1 August 2017

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author name string

Tamary H

1

1 reference

1 August 2017

Shalmon L

2

1 reference

1 August 2017

Shalev H

3

1 reference

1 August 2017

Halil A

4

1 reference

1 August 2017

Dobrushin D

5

1 reference

1 August 2017

Ashkenazi N

6

1 reference

1 August 2017

Zoldan M

7

1 reference

1 August 2017

Resnitzky P

8

1 reference

1 August 2017

Korostishevsky M

9

1 reference

1 August 2017

Bonne-Tamir B

10

1 reference

1 August 2017

Zaizov R

11

1 reference

1 August 2017

language of work or name

English

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publication date

1 May 1998

1 reference

American Journal of Human Genetics

1 August 2017

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1 August 2017

62

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1 August 2017

1062-1069

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1 August 2017

5

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Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Dyserythropoiesis and congenital dyserythropoietic anaemias

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

The gene for human erythrocyte protein 4.2 maps to chromosome 15q15

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Neonatal manifestations of congenital dyserythropoietic anemia type I

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Mapping Using Linkage Disequilibrium Estimates: A Comparative Study

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377091

Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts

9 December 2018

1 reference

12 December 2020

Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25

1 reference

12 December 2020

Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I

1 reference

12 December 2020

Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA-II)

1 reference

12 December 2020

Identifiers

DOI

10.1086/301834

1 reference

release_5jesdgwmwnb7zfhxzuirheaply

1 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/5jesdgwmwnb7zfhxzuirheaply

24 November 2022

mapped directly with Wikidata item

PMCID

1377091

1 reference

1 August 2017

1 reference