Results 61 to 70 of about 835 (101)

[Partial trisomy 9p syndrome: Expanding the phenotype]. [PDF]

Rev Med Inst Mex Seguro Soc
Pérez-Castillo JA, Reyes-Rosales M, Cardoso-Enciso HR, Rodríguez-Cuevas JL.   +3 more
europepmc   +1 more source

Cri du Chat Syndrome and congenital dislocation of the hips and knees: case report. [PDF]

Rev Fac Cien Med Univ Nac Cordoba
Graça NNJ, Ribeiro MLA, Duarte ML.
europepmc   +1 more source

Immature nasopharyngeal teratoma with prenatal diagnosis: Case report and review of the literature [PDF]

Rev Colomb Obstet Ginecol, 2023
Meneses-Parra AL, Tarazona-Bueno RE, Aragón-Mendoza RL, Altman-Restrepo M.   +3 more
europepmc   +1 more source

Medical care in clinical genetics: an experience of decentralization in southern Brazil. [PDF]

Einstein (Sao Paulo), 2021
Meneghini KFD, Karam SM, Madruga VFP, Ungaretti ASS, Pinguello EC, Severo R.   +5 more
europepmc   +1 more source

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

Rev Med Inst Mex Seguro Soc
Crisanto-López IE, García-González R, Saldaña-Guerrero MP, Hernández-Camacho RM, Castro-Coyotl DM.   +4 more
europepmc   +1 more source

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

Rev Paul Pediatr, 2021
Farias MG, Freitas PAC, Spagnol F, Souza MV, Alegretti AP, Riegel M, Taniguchi ANR, Daudt LE.   +7 more
europepmc   +1 more source

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

Rev Colomb Obstet Ginecol, 2022
Gómez-Rojas S, Aristizábal-Duque JE, Muñoz-Fernández LF, Sarmiento-Ramón MP, Pereira-Gómez MDP.   +4 more
europepmc   +1 more source

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

Rev Neurol
Hernández Yeneris SM, González-Solano MA, Lince-Rivera I, Rojas-Martínez JA, Ramón-Gómez JL.   +4 more
europepmc   +1 more source

Karyotype Description of Two Andean Species of the guarani Group of Drosophila (Díptera: Drosophilidae) and Cytological Notes. [PDF]

J Insect Sci, 2021
Vela D, Villavicencio E.
europepmc   +1 more source

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

Rev Neurol, 2022
Nogueira M, Melo C, Grangeia A, Magalhães T, Soares C, Dias R, Fonseca J, Sampaio M, Sousa R.   +8 more
europepmc   +1 more source