(Q53882915)

22 May 2018

title

Is SHORT syndrome another phenotypic variation of PITX2? (English)

1 reference

22 May 2018

1 reference

Nadide Nilüfer Karadeniz

1

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22 May 2018

Inci Kocak-Midillioglu

2

1 reference

22 May 2018

Derya Erdogan

3

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22 May 2018

Isik Bökesoy

4

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22 May 2018

language of work or name

English

0 references

publication date

1 November 2004

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22 May 2018

American Journal of Medical Genetics

published in

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22 May 2018

volume

130A

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22 May 2018

issue

4

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22 May 2018

page(s)

406-409

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22 May 2018

Axenfeld-Rieger syndrome in the age of molecular genetics

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

A molecular basis for differential developmental anomalies in Axenfeld-Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

What is polycystic ovarian syndrome? A proposal for a consensus on the definition and diagnosis of polycystic ovarian syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

Decreased insulin receptor (IR) autophosphorylation in fibroblasts from patients with PCOS: effects of serine kinase inhibitors and IR activators.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

American College of Medical Genetics statement of diagnostic testing for uniparental disomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30206

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.30206

1 reference

22 May 2018

1 reference

22 May 2018