Three new patients with FATCO: Fibular agenesis with ectrodactyly-Reference-Cited by-同舟云学术

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Three new patients with FATCO: Fibular agenesis with ectrodactyly

Published:2012-05-24 Issue:7 Volume:158A Page:1542-1550
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bieganski Tadeusz,Jamsheer Aleksander,Sowinska Anna,Baranska Dobromila,Niedzielski Kryspin,Kozlowski Kazimierz,Czarny-Ratajczak Malwina

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35369/fullpdf

Reference34 articles.

1. X-chromosomally inherited split-hand/split foot anomaly in a Pakistani kindred;Ahmad;Hum Genet,1987

2. Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance;Blattner;Am J Med Genet Part A,2010

3. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: Case report and review;Boles;Am J Med Genet,1995

4. Prenatal diagnosis of femur-fibula-ulna complex by ultrasonography in a male fetus at 24 weeks of gestation;Capece;Prenatal Diag,1994

5. Manifestation of the limb prepattern: Limb development in the absence of sonic hedgehog function;Chiang;Dev Biol,2001

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. A Case of Fibular Aplasia-Tibial Campomelia-Oligosyndactyly (FATCO) Syndrome Associated With Split Hand/Foot Syndrome With Long Bone Deficiency (SHFLD) and Review of the Literature;Cureus;2024-07-22

2. New pathogenic variant in DLX5: New clues for a clinical spectrum from split-hand-foot malformation to fibular aplasia, tibial campomelia and oligosyndactyly;Frontiers in Genetics;2023-04-13

3. Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome;American Journal of Medical Genetics Part A;2023-01-06

4. A case report on Fibular Aplasia, Tibial Campomelia, Oligosyndactyly Syndrome variant in a Male Infant;Journal of the Pakistan Medical Association;2022-05-10

5. Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight;Cureus;2022-01-28

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