(Q34745523)

4 August 2017

title

Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions (English)

1 reference

4 August 2017

Wright TJ

1

1 reference

4 August 2017

Clemens M

series ordinal

2

1 reference

4 August 2017

Quarrell O

series ordinal

3

1 reference

4 August 2017

Altherr MR

series ordinal

4

1 reference

4 August 2017

publication date

1 February 1998

1 reference

American Journal of Medical Genetics Part A

4 August 2017

published in

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4 August 2017

volume

75

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4 August 2017

issue

4

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4 August 2017

page(s)

345-350

1 reference

Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?

21 January 2018

1 reference

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 January 2018

1 reference

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Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.

21 January 2018

1 reference

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Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans

21 January 2018

1 reference

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A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

A common FGFR3 gene mutation in hypochondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

Report on trisomies 18 and a trisomy 18 mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980203%2975%3A4%3C345%3A%3AAID-AJMG2%3E3.0.CO%3B2-P

10.1002/(SICI)1096-8628(19980203)75:4<345::AID-AJMG2>3.0.CO;2-P

21 January 2018

Identifiers

DOI

1 reference

4 August 2017

1 reference