Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation
Author:
Affiliation:
1. Quaid-i-Azam University, Pakistan
2. BUITEMS, Pakistan
3. Khushal Khan Khattak University, Pakistan
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v41n1/1415-4757-gmb-1678-4685-GMB-2016-0162.pdf
Reference29 articles.
1. Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families;Aziz A;Gene,2014
2. Homozygous nonsense mutation in WNT10B and sporadic split-hand/foot malformation (SHFM) with autosomal recessive inheritance;Blattner A;Am J Med Genet A,2010
3. Deletion of chromosome 2q24-q31 causes characteristic digital anomalies: case report and review;Boles RG;Am J Med Genet,1995
4. Pathogenesis of split-hand/split-foot malformation;Duijf PH;Hum Mol Genet,2003
5. Genotype-phenotype correlations in mapped split hand foot malformation (SHFM) patients;Elliott AM;Am J Med Genet,2006
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