Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: Genetic homogeneity and nosological delineation-Reference-Cited by-同舟云学术

Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: Genetic homogeneity and nosological delineation

Published:2010-12-22 Issue:2 Volume:155 Page:332-336
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Garavelli Livia,Wischmeijer Anita,Rosato Simonetta,Gelmini Chiara,Reverberi Sandro,Sassi Silvia,Ferrari Adriano,Mari Francesca,Zabel Bernhard,Lausch Ekkehart,Unger Sheila,Superti-Furga Andrea

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33793/fullpdf

Reference25 articles.

1. No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome;Abo-Dalo;Clin Dysmorphol,2008

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

3. Congenital duplication of the palm syndrome: Gene analysis and the molecular basis of its clinical features;Al-Qattan;J Hand Surg Eur,2009

4. Novel human pathological mutations. Gene symbol: WNT7A. Disease: Ulnar and fibula absence, with severe limb deficiency;Al-Balwi;Hum Genet,2009

5. Limb/pelvis-hypoplasia/aplasia syndrome (Al-Awadi/Raas-Rothschild syndrome): Report of two Italian sibs and further confirmation of autosomal recessive inheritance;Camera;J Med Genet,1993

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mammalian uterine morphogenesis and variations;Current Topics in Developmental Biology;2022

2. Dorsal–Ventral Deficiency;Congenital Anomalies of the Upper Extremity;2021

3. WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders;Frontiers in Endocrinology;2020-04-09

4. Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases;Journal of Cellular Biochemistry;2019-07-04

5. WNT7A (rs104893832) polymorphism increases the risk of recurrent spontaneous abortion in Iranian women;Universa Medicina;2018-09-13