Results 141 to 150 of about 3,131 (193)

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

Prevalence and clinical characterization of oral clefts in patients with chromosome trisomy 18. [PDF]

Rev Paul Pediatr
Martinez NCM, Almeida ST, Rosa RFM, Zen PRG.   +3 more
europepmc   +1 more source