Results 91 to 100 of about 355 (156)

[Epilepsy and inborn errors of metabolism]. [PDF]

Rev Neurol
Moya-López S, Ruiz-Colodrero A, Sainz-García J, Fariña-Jara V, García-Jiménez MC, Castejón-Ponce E, López-Pisón J, Pérez-Delgado R.   +7 more
europepmc   +1 more source

Exogenous pigmentation by silver nitrate: Dermatological and toxicological aspects, case report

Biomedica, 2021
Londoño Á, Pérez C, Restrepo R, Morales N, Martínez M, Morales D.   +5 more
europepmc   +1 more source

Consanguinidad y proporción de sexos en un núcleo cerrado de ganado porcino

, 2018
[EN] The sex ratio in a closed herd of Large White swine, computed from 25,125 piglets in 2,383 litters, was 53.90% of males for the period 1931-85. Within each litter size sex ratio fits satisfactorily well to a binomial distribution for a sex ratio of 54% of males/46% of females.
openaire   +1 more source

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

Rev Med Inst Mex Seguro Soc
Crisanto-López IE, Saldaña-Guerrer MP, Hernández-Camacho RM, Castro-Coyotl DM.   +3 more
europepmc   +1 more source

Consanguinidade

, 1905
openaire   +2 more sources

Efecto de la consanguinidad sobre las características económicas del ganado criollo lechero

, 2014
Tesis (M.
openaire   +1 more source

Agregación familiar y factores de riesgo de cáncer de próstata en individuos afectados

Revista Finlay
Fundamento: el cáncer de próstata constituye la segunda causa de muerte en el hombre a nivel mundial. Estudios genéticos señalan un vínculo entre ciertas mutaciones genéticas, la agresividad de esta neoplasia, el riesgo de desarrollar la enfermedad y las
Julio Armando Sánchez Delgado, Nailé Edita Sánchez Lara   +1 more
doaj  

Genetic and radiological aspects of pediatric renal cystic disease: A case series [PDF]

Biomedica
Pacheco-Orozco RA, Forero-Delgadillo JM, Ochoa V, Toro JS, Pachajoa H, Restrepo JM.   +5 more
europepmc   +1 more source

Capítulo VI a consanguinidade e o parentesco

, 1992
openaire   +1 more source

First report of PURA syndrome in a Colombian patient with de novo missense variant c.692T>C (p.Phe231Ser) [PDF]

Biomedica
Cerón SM, Pérez DA, Montaño JH, Acosta MA.   +3 more
europepmc   +1 more source