Literature DB >> 7337959

Limb deficiency syndrome in half-sibs.

J T Hecht, C I Scott.   

Abstract

Entities:  

Mesh：

Year:  1981        PMID： 7337959     DOI： 10.1111/j.1399-0004.1981.tb01054.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  6 in total

1.  A Turkish Female Twin Sister Patient with Fibular Aplasia, Congenital Tibia Pseudoarthrosis, Oligosyndactyly, and Negative WNT7A Gene Mutation.

Authors:  Hale Önder Yılmaz; Duran Topak; Orkun Yılmaz; Seda Çakmaklı
Journal:  J Pediatr Genet       Date:  2018-11-18

2.  Familial combination of brachydactyly, type E and atrial septal defect, type II.

Authors:  A Czeizel; P Göblyös
Journal:  Eur J Pediatr       Date:  1989-11       Impact factor: 3.183

3.  Overlap between Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly and Fuhrmann's Syndromes in an Egyptian Female Infant.

Authors:  Ebtesam M Abdalla; Ahmed A El-Beheiry
Journal:  J Pediatr Genet       Date:  2017-01-02

4.  A Female Newborn Infant with FATCO Syndrome Variant (Fibular Hypoplasia, Tibial Campomelia, Oligosyndactyly) - A Case Report.

Authors:  Gitte Smets; Yoeri Vankan; Annick Demeyere
Journal:  J Belg Soc Radiol       Date:  2016-02-26       Impact factor: 1.894

5.  Fibular Hypoplasia, Talar Aplasia, Absent Proximal Tibial Growth Plate and Oligosyndactyly (Variant of Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome) - Paucity of Case Reports with Evolving Definition.

Authors:  Pankaj Kumar Mishra; Maneesh Verma
Journal:  J Orthop Case Rep       Date:  2021-08

6.  Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight.

Authors:  Marian K Georgeos; Dina R Elgzzar
Journal:  Cureus       Date:  2022-01-28
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.