Fine mapping of the Autosomal Dominant Split Hand/Split Foot Locus on Chromosome 7, Band q21.3-q22.1

Split hand/split foot (SHFD) is a human developmental defect characterized by missing digits, fusion of remaining digits, and a deep median cleft in the hands and feet. Cytogenetic studies of deletions and translocations associated with this disorder have indicated that an autosomal dominant split h...

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Bibliografiset tiedot
Päätekijät: Scherer, Stephen W., Poorkaj, Parvoneh, Allen, Todd, Kim, Julia, Geshuri, Dorrit, Nunes, Mark, Soder, Sylvia, Stephens, Karen, Pagon, Roberta A., Patton, Michael A., Berg, Mary Anne, Donlon, Tim, Rivera, Horacio, Pfeiffer, R. A., Naritomi, Kenji, Hughes, Helen, Genuardi, Maurizio, Gurrieri, Fiorella, Neri, Giovanni, Lovrein, Everett, Magenis, Ellen, Tsui, Lap-Chee, Evans, James P.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1994
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Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918243/
https://ncbi.nlm.nih.gov/pubmed/8023840
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