Results 141 to 150 of about 711 (175)

Molecular spectrum and differential diagnosis in patients referred with sporadic or autosomal recessive osteogenesis imperfecta. [PDF]

open access: yesMol Genet Genomic Med, 2017
Caparros-Martin JA   +24 more
europepmc   +1 more source

Genetics and genomic medicine in the Philippines. [PDF]

open access: yesMol Genet Genomic Med, 2016
Padilla CD, Cutiongco-de la Paz EM.
europepmc   +1 more source

A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report. [PDF]

open access: yesJ Med Case Rep, 2016
Ramos-Zaldívar HM   +17 more
europepmc   +1 more source

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