Results 121 to 130 of about 5,203 (149)

Bilateral ulnar longitudinal deficiency with oligodactyly in newborn. [PDF]

open access: yesRev Paul Pediatr
Simão SCM   +5 more
europepmc   +1 more source

Myelodysplastic syndrome: validation of flow cytometry multilineage score system. [PDF]

open access: yesEinstein (Sao Paulo), 2020
Araújo HV   +11 more
europepmc   +1 more source

Análise citogenéticade gymnotiformescomercializados como iscas vivas no rio paraguai, Porto da manga, MS. [PDF]

open access: yes, 2012
MARQUES, D. K. S.   +3 more
core  

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

open access: yesSci Rep
Duque A   +5 more
europepmc   +1 more source

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

open access: yesRev Paul Pediatr
Nisihara R   +6 more
europepmc   +1 more source

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

open access: yesRev Paul Pediatr
Anacleto PZ   +2 more
europepmc   +1 more source

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

open access: yesRev Med Inst Mex Seguro Soc
Jiménez-Pérez B   +6 more
europepmc   +1 more source

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