Results 241 to 250 of about 157,575 (291)
Unusual Disease‐Progression in Two Siblings With Xeroderma Pigmentosum Group G
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
Improving overall child survival in conflict and fragile settings via integration of medical innovations into broader health system strengthening efforts: lessons from six rural hospitals in Somalia. [PDF]
Saidu Y, Ngenge BM, Rudan I.
europepmc +1 more source
Levels and determinants of child wasting relapse: a prospective cohort study from Somalia. [PDF]
Alier KK +19 more
europepmc +1 more source
Prevalence and motivation factors of bleaching practices among female university students in Mogadishu, Somalia. [PDF]
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]
Ali MN +12 more
europepmc +1 more source
Measles outbreak associated with an infectious travel. [PDF]
Adan AM +4 more
europepmc +1 more source
Africa Economic Brief - Economic Impact of Maritime Piracy [PDF]
Mbekeani, Kennedy K., Ncube, Mthuli
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