Results 101 to 110 of about 1,238,800 (147)

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder. [PDF]

open access: yesNat Genet
Greene D   +30 more
europepmc   +1 more source

Mutational spectrum of SLC26A4 and SLC26A5 associated with hereditary hearing loss in Moroccan families. [PDF]

open access: yesHum Genomics
Idyahia A   +6 more
europepmc   +1 more source

Coping Strategies and Social Support for Transition Readiness Among Youth With Sickle Cell Disease.

open access: yesJAMA Netw Open
Iyengar AS   +16 more
europepmc   +1 more source

Emergence of rare SARS-CoV-2 subvariant LF.7.3 obtained from Moroccan COVID-19 patients. [PDF]

open access: yesMicrobiol Resour Announc
Ghammaz H   +6 more
europepmc   +1 more source

Anaesthesiologists Under Strain: Burnout and Its Associated Factors in a Conflict-affected Context, a Cross-sectional Study. [PDF]

open access: yesTurk J Anaesthesiol Reanim
Yazbeck Karam V   +11 more
europepmc   +1 more source

Early-Onset Type 2 Diabetes: A Comprehensive Review From Adolescence to Adulthood. [PDF]

open access: yesCureus
Alomari NA   +8 more
europepmc   +1 more source

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