(Q53493173)

14 May 2018

title

Polymicrogyria in a 10-month-old boy with Mowat-Wilson syndrome. (English)

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14 May 2018

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Susan B Murray

1

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14 May 2018

Brooke B Spangler

series ordinal

2

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14 May 2018

Benjamin M Helm

series ordinal

3

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14 May 2018

Samantha Schrier Vergano

series ordinal

4

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14 May 2018

language of work or name

English

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publication date

26 May 2015

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14 May 2018

American Journal of Medical Genetics

published in

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14 May 2018

volume

167A

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14 May 2018

issue

10

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14 May 2018

page(s)

2402-2405

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14 May 2018

Clinical features and management issues in Mowat-Wilson syndrome.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

ZFHX1B mutations in patients with Mowat-Wilson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

21 January 2018

Mowat-Wilson syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Mowat-Wilson syndrome: facial phenotype changing with age: study of 19 Italian patients and review of the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat-Wilson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Malformations of cortical development: clinical features and genetic causes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

21 January 2018

Mowat-Wilson syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Mowat-Wilson syndrome in a fetus with antenatal diagnosis of short corpus callosum: advocacy for standard autopsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Polymicrogyria: a common and heterogeneous malformation of cortical development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37171

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.37171

1 reference

14 May 2018

PubMed ID

26012591

1 reference

14 May 2018