(Q28187677)

2

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Memnune Yüksel-Apak

5

object named as

Memnune Yuksel-Apak

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author name string

Oya Uyguner

3

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Turgut Tukel

The ulnar-mammary syndrome: an autosomal dominant pleiotropic gene

4

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language of work or name

English

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publication date

2002

1 reference

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45

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issue

4

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page(s)

213-7

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Clinical analysis of a large kindred with the Pallister ulnar-mammary syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Brachyury and the T-box genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

7 January 2021

The T-box gene family

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

A combined analysis of genomic and primary protein structure defines the phylogenetic relationship of new members if the T-box family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9

7 January 2021

Ulnar-mammary syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2802%2901144-9