Results 131 to 140 of about 7,482 (176)

[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

[Inequalities in time to diagnosis of Down Syndrome in Bolivia]. [PDF]

open access: yesSalud Colect
Linares Terrazas D   +2 more
europepmc   +1 more source

RECOMENDAÇÕES PARA O DIAGNÓSTICO, TRATAMENTO E MONITORIZAÇÃO DA LEUCEMIA MIELÓIDE CRÓNICA. [PDF]

open access: yes, 2009
Almeida, A.   +5 more
core  

Fertilidade na Síndrome de Turner [PDF]

open access: yes, 2015
Catarina Ribeiro Costa
core  

First report of hypoplastic left heart syndrome in 3p- syndrome and review of candidate genes. [PDF]

open access: yesRev Paul Pediatr
Böttcher AK   +7 more
europepmc   +1 more source

Jacobsen syndrome associated with Shone's complex: a case report. [PDF]

open access: yesRev Paul Pediatr
Brum A   +3 more
europepmc   +1 more source

Characterization of patients treated at a rare disease referral service: a descriptive study, 2016-2021. [PDF]

open access: yesEpidemiol Serv Saude
Carvalho EA   +10 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy