Results 61 to 70 of about 126,587 (112)

<i>APOL1</i> G1/G2 Variants Associated With CKD in Afro-Brazilians. [PDF]

Kidney Int Rep
Souza CMB, Fam BSO, Giudicelli GC, Cadore NA, Feira MF, Prado MJ, Kowalski TW, Artigalás OAP, Lemes RB, Rodrigues MR, Junior MRS, Silva WC, Torely MD, Barbosa FM, da Costa Pereira A, Pereira LV, Hünemeier T, Veronese FV, Vianna FSL.   +18 more
europepmc   +1 more source

La regulación jurídica de la manipulación genética [PDF]

, 1999
García Miranda, Carmen María
core  

Geographic and Socioeconomic Determinants of Treatment Abandonment in Pediatric Acute Leukemia: A Cohort Study in South-Central Mexico. [PDF]

Cancer Control
Núñez-Enriquez JC, Luna-Silva NC, Jacuinde-Trejo K, Flores-Lujano J, Medina-León D, Alarcón-Ruiz E, Garrido-Hernández MÁ, Cruz-Medina CS, Tinoco-Montejano D, Baños-Lara MDR, Campo-Martínez MLÁD, Duarte-Rodríguez DA, Allende-López A, Casique-Aguirre D, Elizarrarás-Rivas J, Olvera-Caraza D, Solís-Poblano JC, Terán-Cerqueda V, Ramírez-Ramírez D, Huerta-Moreno A, Aristil-Chery PM, Romo-Rodríguez R, Alvarez-Rodríguez E, Lien-Chang LEJ, Zamora-Herrera G, Hidalgo BG, Herrera-Olivares W, Ruíz-Arguelles GJ, Gallardo-Pérez MM, Chávez-Aguilar LA, Márquez-Toledo A, Cano-Cuapio LS, Ramos RH, Martínez-Martell MA, Ramirez-Ramirez AB, Brindis NR, Montiel-Jarquín AJ, Galván-Díaz CA, Velasco-Hidalgo L, Medina-Sanson A, Gutiérrez-Rivera ML, Cárdenas-Conejo A, Morales-Maravilla A, Victorio-García NP, Bekker-Méndez VC, Romero-Tlalolini MLÁ, Rodríguez-Espinosa JC, Mata-Rocha M, Olivares-Sosa AI, Rosas-Vargas H, Jiménez-Morales S, Martínez MEJ, Cárdenas-González M, Mejía-Aranguré JM, López-Aguilar E, Zapata-Tarrés M, Pelayo R.   +56 more
europepmc   +1 more source

Unveiling Mucopolysaccharidosis IIIC in Brazil: Diagnostic Journey and Clinical Features of Brazilian Patients Identified Through the MPS Brazil Network. [PDF]

Diseases
Montenegro YHA, Alves MFA, Santos-Lopes SSD, Souza CFM, Poswar FO, Brusius-Facchin AC, Bender-Pasetto F, Michelin-Tirelli K, Sebastião FM, Trapp FB, Ribeiro EM, Medeiros PFV, Kim CA, Embiraçu EK, Riegel-Giugliani M, Baldo G, Giugliani R.   +16 more
europepmc   +1 more source

Isolated Follicle-Stimulating Hormone (FSH) Deficiency in Male Sex: A Case Report. [PDF]

Cureus
Soares DM, Silva JD, Soares AR, Couto de Carvalho A.   +3 more
europepmc   +1 more source

Investigação das causas genéticas de doenças primárias do músculo: a experiência da unidade de genética molecular do CGMJM [PDF]

, 2013
Gonçalves, A., Maia, N., Oliveira, J., Oliveira, M., Santos, R., Vieira, E.   +5 more
core  

Comparative analysis of PRR receptors and R genes reveals structural and functional divergence between wild, ancestral, and commercial citrus species. [PDF]

BMC Genomics
Dos Santos Menezes F, Silva RJS, Ollitrault P, Micheli F.   +3 more
europepmc   +1 more source

Correction: Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant. [PDF]

Eur J Hum Genet
Daga S, Loberti L, Rollo G, Adamo L, Colavecchio OL, Brunelli G, Zguro K, Tripodi SA, Guarnieri A, Garosi G, D'Aurizio R, Ariani F, Tita R, Renieri A, Pinto AM.   +14 more
europepmc   +1 more source

La terapia genética: observaciones para una perspectiva ética [PDF]

, 1993
Ruiz-Pérez, G. (Gregorio)
core  

Erratum in: Abnormal Splicing in the Final Intron of PRX Results in Dominant Congenital Cataract Without Neurological Phenotype. [PDF]

Invest Ophthalmol Vis Sci
europepmc   +1 more source