Results 101 to 110 of about 1,232 (182)

[20q11.2 microdeletion syndrome: a phenotypic spectrum expansion. Case report]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Crisanto-López IE   +4 more
europepmc   +1 more source

HEMOPHAGOCYTOSIS BY BLASTS IN A CHILD WITH ACUTE MONOCYTIC LEUKEMIA AFTER CHEMOTHERAPY. [PDF]

open access: yesRev Paul Pediatr, 2021
Farias MG   +7 more
europepmc   +1 more source

New STAG3 gene variant as a cause of premature ovarian insufficiency [PDF]

open access: yesRev Colomb Obstet Ginecol, 2022
Gómez-Rojas S   +4 more
europepmc   +1 more source

[Neurodevelopmental and Movement Disorder Due to a Mutation in the GNAO1 Gene: A Case Report]. [PDF]

open access: yesRev Neurol
Hernández Yeneris SM   +4 more
europepmc   +1 more source

PURA syndrome in a child with severe developmental delay: a challenging diagnosis. [PDF]

open access: yesRev Neurol, 2022
Nogueira M   +8 more
europepmc   +1 more source

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