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Browsing by Author Cohn, DH
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Showing results 3 to 5 of 5
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Title
Author(s)
Issue Date
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)
Journal:
Clinical Genetics
FaiyazUlHaque, M
Ahmad, W
Zaidi, SHE
Haque, S
Teebi, AS
Ahmad, M
Cohn, DH
Tsui, LC
2002
Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis)
Journal:
Clinical Genetics
FaiyazUlHaque, M
Ahmad, W
Zaidi, SHE
Hussain, S
Haque, S
Ahmad, M
Cohn, DH
Tsui, LC
2004
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
Journal:
Journal of Medical Genetics
Aldinger, KA
Mendelsohn, NJ
Chung, BHY
Zhang, W
Cohn, DH
Fernandez, B
Alkuraya, FS
Dobyns, WB
Curry, CJ
2016