Results 101 to 110 of about 5,203 (149)

[Ring chromosome 21 syndrome: report of 2 cases]. [PDF]

Rev Med Inst Mex Seguro Soc
Guzmán-Santiago TA, Juárez-Melchor D, Jiménez-Pérez B, Vera-Loaiza A, Pérez-Arzola AA, Hernández-Castañeda Y, Rodríguez-Hurtado PO, Crisanto-López IE, Garduño-Zarazúa LM, Salazar-Bonilla W.   +9 more
europepmc   +1 more source

[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

[Congenital heart disease in Down's syndrome]. [PDF]

Arch Cardiol Mex, 2023
Arias-Lobo R, Lupinta-Paredes E, Calderón-Colmenero J, Cervantes-Salazar JL, García-Montes JA, Patiño-Bahena EJ, Benita-Bordes A.   +6 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

Diagnóstico e benefícios para a comunidade na doença genética: contributo da citogenética [PDF]

, 2013
Aguiar, J., Fortuna, A., Freitas, M., Lopes, E., Marques, B., Oliva-Teles, N., Silva, M.   +6 more
core  

[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