(Q52115268)

22 April 2018

title

Wolcott-Rallison syndrome in two siblings with isolated central hypothyroidism. (English)

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22 April 2018

Wolcott-Rallison syndrome

1 reference

1 reference

Bassam Bin-Abbas

1

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22 April 2018

Abdulmohsen Al-Mulhim

series ordinal

2

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22 April 2018

Abdullah Al-Ashwal

series ordinal

3

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22 April 2018

publication date

1 August 2002

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22 April 2018

American Journal of Medical Genetics Part A

published in

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22 April 2018

volume

111

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22 April 2018

issue

2

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22 April 2018

page(s)

187-190

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22 April 2018

Organisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndrome

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10495

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10495

Wolcott-Rallison syndrome: diabetes mellitus and spondyloepiphyseal dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10495

Paternal uniparental disomy for chromosome 6 causes transient neonatal diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10495

21 January 2018

Identifiers

DOI

10.1002/AJMG.10495

1 reference

22 April 2018

PubMed ID

12210348

1 reference

22 April 2018