Results 191 to 200 of about 20,090 (253)

c.7156C > T p.(Gln2386*) variant causes loss-of-function of the USP9X gene in a female-restricted X-linked syndromic intellectual disability: a case report. [PDF]

open access: yesJ Med Case Rep
da Silva Campos TA   +7 more
europepmc   +1 more source

The hip desis for untreated congenital dislocation of the hip.

open access: diamond, 1984
K. Akasaki   +6 more
openalex   +2 more sources

A Rare Case of Bilateral Congenital Radial Head Dislocation: A Case Report. [PDF]

open access: yesJ Orthop Case Rep
Gultekin O   +4 more
europepmc   +1 more source

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