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Molecular basis of the clinical features of Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome (AARRS) and Fuhrmann syndrome

  • Published:2013-08-06 Issue:9 Volume:161 Page:2274-2280
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am. J. Med. Genet.

Author:

Al-Qattan M.M.1

Affiliation:

1. Division of Plastic Surgery; King Saud University; Riyadh Saudi Arabia

Funder

College of Medicine Research Center, Deanship of Scientific Research, King Saud University, Riyadh, Saudi Arabia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. En l and WNT7A interact with DKK1 during limb development in the mouse;Adamska;Develop Biol,2004

2. Profound limb deficiency, thoracic dystrophy, unusual facies and normal intelligence: A new syndrome;Al-Awadi;J Med Genet,1985

3. Al-Awadi/Raas-Rothschild syndrome in a new born with additional anomalies;Alp;J Clin Res Ped Endo,2010

4. Congenital duplication of the palm in a patient with multiple anomalies;Al-Qattan;J Hand Surg Br,2003

5. WNT pathways and upper limb anomalies;Al-Qattan;J Hand Surg Eur,2011

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