Results 91 to 100 of about 410,966 (143)

[KIF1A gene-associated neurological disease: the correlation between genotype and phenotype]. [PDF]

open access: yesRev Neurol, 2023
Ortiz-Ortigosa A   +4 more
europepmc   +1 more source

[Spinal muscular atrophy: Clinical and genetic aspects, and therapeutic alternatives]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
González-Morales IJ   +3 more
europepmc   +1 more source

[Rh blood group: Review and importance of genotyping]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Campos-Aguirre E   +3 more
europepmc   +1 more source

Prenatal diagnosis of Freeman-Sheldon syndrome using ultrasound and genetic testing. Case report [PDF]

open access: yesRev Colomb Obstet Ginecol, 2023
Annicchiarico-López W   +2 more
europepmc   +1 more source

[Lactose Malabsorption and Intolerance]. [PDF]

open access: yesActa Gastroenterol Latinoam
Ordoñez-Vázquez AL   +2 more
europepmc   +1 more source

[Correlation of anxiety in parents and children with attention deficit/hyperactivity disorder]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
García-Galicia A   +7 more
europepmc   +1 more source

[Screening of Hepatitis C virus in blood donors over 11 years]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Rodríguez-Rivera JL   +2 more
europepmc   +1 more source

[Clinical and genetic characterisation of hereditary distal myopathies in a series of Colombian patients]. [PDF]

open access: yesRev Neurol
Oliveros-Acuña N   +5 more
europepmc   +1 more source

[BCL11B associated disorder a case report in Mexican population. Case report]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Crisanto-López IE   +3 more
europepmc   +1 more source

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