(Q28244960)

1

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T N Willing

2

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A van Haeringen

3

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G Tchernia

4

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I Dianzani

5

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M Donnér

6

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G Elinder

7

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J I Henter

8

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P G Nilsson

9

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L Gordon

10

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G Skeppner

11

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L van't Veer-Korthof

12

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A Kreuger

13

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N Dahl

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

14

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language of work or name

English

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publication date

August 1997

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published in

Nature Genetics

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volume

16

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issue

4

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page(s)

368-71

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0897-368

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0897-368

Diamond-Blackfan anaemia in the U.K.: analysis of 80 cases from a 20-year birth cohort.

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

An integrated metric physical map of human chromosome 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

Diamond-Blackfan anemia. Natural history and sequelae of treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Heterogeneity of the erythropoietic defect in two cases of Aase-Smith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Long-term survival and cure after marrow transplantation for congenital hypoplastic anaemia (Diamond-Blackfan syndrome).

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Report an abstracts of the third international workshop on human chromosome 19 mapping 1996.

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Elevated red cell adenosine deaminase activity: a marker of disordered erythropoiesis in Diamond-Blackfan anaemia and other haematologic diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Congenital hypoplastic anemia: another example of autosomal dominant transmission

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1 reference

https://api.crossref.org/works/10.1038%2FNG0897-368

7 January 2021

Identifiers

DOI

10.1038/NG0897-368

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

9241274

1 reference

Consolidated OpenCitations Corpus – April 2017