Results 81 to 90 of about 845 (101)

Metabolic dysfunction-associated liver disease and biliary lithiasis in children with Down Syndrome: a retrospective study. [PDF]

Rev Paul Pediatr
Nisihara R, Fuga NH, Maia L, Mansur MG, Liberatti F, Rossasi M, Oliveira N.   +6 more
europepmc   +1 more source

[Rare diseases in a medical genetics service of population with social security]. [PDF]

Rev Med Inst Mex Seguro Soc
Jiménez-Pérez B, Juárez-Melchor D, Guzmán-Santiago AA, Sánchez-Ortega A, Vera-Loaiza A, Flores-Martínez C, Aguilar-Cózatl I.   +6 more
europepmc   +1 more source

An integrated approach for rare disease detection and classification in Spanish pediatric medical reports. [PDF]

Sci Rep
Duque A, Araujo L, Martinez-Romo J, Esteban-Vasallo MD, Domínguez-Berjón MF, Malillos Perez D.   +5 more
europepmc   +1 more source

Trisomy 13, home health-care and multidisciplinary approach: Case report. [PDF]

Rev Paul Pediatr
Anacleto PZ, Sousa VA, Joviano-Santos JV.   +2 more
europepmc   +1 more source

Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype. [PDF]

Einstein (Sao Paulo), 2016
Pratte-Santos R, Ribeiro KH, Santos TA, Cintra TS.   +3 more
europepmc   +1 more source

Non-coding rnas in Turner syndrome: a systematic review. [PDF]

Rev Paul Pediatr
Oliveira JCC, Barbosa EDS, Silva NB, Silva TDC, Matos AGM, Pinho JD.   +5 more
europepmc   +1 more source