Results 241 to 250 of about 157,575 (291)

Unusual Disease‐Progression in Two Siblings With Xeroderma Pigmentosum Group G

open access: yesClinical Genetics, Volume 109, Issue 5, Page 984-985, May 2026.
Protein truncation mutations in the gene for XPG nuclease cause a very severe clinical phenotype. Two siblings have splicing mutations, which result in in‐frame deletions and a less severe phenotype.
Elena Botta   +4 more
wiley   +1 more source

Levels and determinants of child wasting relapse: a prospective cohort study from Somalia. [PDF]

open access: yesJ Glob Health
Alier KK   +19 more
europepmc   +1 more source

Prevalence and motivation factors of bleaching practices among female university students in Mogadishu, Somalia. [PDF]

open access: yesSAGE Open Med
Ahmed NR   +8 more
europepmc   +1 more source

Waardenburg-Shah Syndrome: Diagnostic and Surgical Challenges in a Resource-Limited Setting - A Rare Case Report. [PDF]

open access: yesInt Med Case Rep J
Ali MN   +12 more
europepmc   +1 more source

Measles outbreak associated with an infectious travel. [PDF]

open access: yesTrop Dis Travel Med Vaccines
Adan AM   +4 more
europepmc   +1 more source

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