Selective chromatid segregation mechanism proposed for the human split hand/foot malformation development by chromosome 2 translocations: A perspective
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,Molecular Biology
Reference46 articles.
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3. A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.1 identified from a chromosome translocation;Babbs;Hum. Genet.,2007
4. Complex rearrangement of chromosomes 7q21.13–q22.1 confirms the ectrodactyly-deafness locus and suggests new candidate genes;Bernardini;Am. J. Med. Genet. Part A,2008
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