The role of ultrasound and genetic counsel in prenatal diagnosis of split hand/foot malformation with long bone deficiency
Author:
Funder
Ministry of Science and Higher Education
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference13 articles.
1. 17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD);Armour;Eur J Hum Genet,2011
2. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion;Klopocki;J Med Genet,2012
3. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3;Lezirovitz;Hum Genet,2008
4. Split-hand/foot malformation - molecular cause and implications in genetic counselling;Sowińska-Seidler;J Appl Genet,2014
5. Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1;Naveed;Am J Hum Genet,2007
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