Výsledky vyhledávání - "Aparicio-Rodríguez JM"

Malformation Variability Associated to Chromosome Trisomies. Clinical and Phenotipical Implications in Several Patients at a Pediatric Hospital in Mexico

Autor: Aparicio-Rodríguez JM, Hurtado-Hernández MdL, Cubillo-León MA, Chatelain-Mercado S

Publikováno v: Journal of Asian Scientific Research. 3(1):85-106

Chromosome trisomies are considered alterations in the chromosome number or structure. A trisomy is therefore a type of polysomy in which there are three chromosome copies, instead of the normal two. A trisomy is considered an aneuploidy or abnormal

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Ring Chromosomes Aberrations at a Pediatric Mexican Hospital. Two Cases with Mosaisism of Chromosome 13, 46XY / 46, XY, R (13) and Chromosome 18, 46, XY / 46, XY, R (18)

Autor: Aparicio-Rodríguez JM, Hurtado-Hernández MdL, Barrientos-Pérez M

Publikováno v: Journal of Asian Scientific Research. 3(2):174-187

The autosomic alteration due to a ring formation is a rare aberration of either chromosome 13 and 18 which is in relation with phenotipic malformations, neurologic problems and genital abnormalities. Two clinical polymalformed cases with skull trebol

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Cell Malignitation Associated To Chromosome Translocations. Clinical Manifestations in Two Pediatric Patients 46,Xy,T(1;4)(Q11q11) and 46,Xy,T(6;9)(P21;Q34)

Autor: Aparicio-Rodríguez JM, Hurtado-Hernández MdL, Chatelain-Mercado S

Publikováno v: Journal of Asian Scientific Research. 3:403-416

The majority of de novo structural chromosome aberrations in fetuses and newborns are considered being of cells of mammals for DNA damage during gametogenesis. 4617 chromosomal studies performed during 19 years (from 1992 to 2011), at Hospital Para E

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Cromosome 4 Deletions and Translocations Among 4617 Cariotype Studies at a Third Level Pediatric Mexican Hospital. 4p-, 4q-, T (1; 4), T (3; 4), Six Cases Report

Autor: Aparicio-Rodríguez JM Manzoor, Hurtado-Hernández MdL, Hernández Lara González FE, Romero Díaz A, Rodríguez-Peralta S, Zamudio-Meneses R, Cuellar-López F, Palma-Guzmán M, Chavez-Ozeki H, Vega Galina VJ, Chatelain-Mercado S

Publikováno v: Journal of Asian Scientific Research. 2(12):866-883

Chromosome aberrations are considered changes in the chromosome number or structure. The etiology factor is due to gametogenesis inborn error (meiosis) or during the zygote first cellular divisions. It might occurs during metaphase from the cellular

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Akademický článek

Juvenile polyposis of infancy associated with paracentric inversion and deletion of chromosome 10 in a Hispanic patient: a case report.

Autor: Vargas-González R; Pathology Department, Hospital Puebla Privada de las Ramblas No 4, CP 72197 Puebla Pue., México. soncoy@msn.com, de la Torre-Mondragón L, Aparicio-Rodríguez JM, Paniagua-Morgan F, López-Hernández G, Garrido-Hernández MA, Nuñez-Barrera S

Publikováno v: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society [Pediatr Dev Pathol] 2010 Nov-Dec; Vol. 13 (6), pp. 486-91. Date of Electronic Publication: 2010 Mar 24.

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