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Isabel Melaragno

Showing results (31-40 of 87) with videos related to

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Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 28, 2014
Congenital adrenal hyperplasia, ovarian failure and Ehlers-Danlos syndrome due to a 6p deletionMariana Moysés-Oliveira, Tatiane I Mancini, Sylvia S Takeno, et al.
Molecular Syndromology|March 22, 2016
22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro FertilizationAnelisa Gollo Dantas, Adriana Bortolai, Mariana Moysés-Oliveira, et al.
Journal of Applied Genetics|December 19, 2012
Ring chromosome 10: report on two patients and review of the literatureRoberta Santos Guilherme, Chong Ae Kim, Luis Garcia Alonso, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Deletion 22q11.2: report of a complex meiotic mechanism of originSintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, et al.
American Journal of Medical Genetics|November 20, 2002
Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequenceJuliana Godoy Assumpção, Windy Berkofsky-Fessler, Nilma Viguetti Campos, et al.
Journal of Molecular Histology|November 24, 2011
Cytogenetic instability of dental pulp stem cell linesMonica Talarico Duailibi, Leslie Domenici Kulikowski, Silvio Eduardo Duailibi, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Human Genetics|December 17, 2015
Incorporation of 5-ethynyl-2'-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangementsLuiza Sisdelli, Angela Cristina Vidi, Mariana Moysés-Oliveira, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 23, 2012
Autistic disorder phenotype associated to a complex 15q intrachromosomal rearrangementDenise Maria Christofolini, Vera Ayres Meloni, Marco Antonio de Paula Ramos, et al.
Pageof 9

Showing results (31-40 of 87) with videos related to

Sort By:
Pageof 9
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|June 28, 2014
Congenital adrenal hyperplasia, ovarian failure and Ehlers-Danlos syndrome due to a 6p deletionMariana Moysés-Oliveira, Tatiane I Mancini, Sylvia S Takeno, et al.
Molecular Syndromology|March 22, 2016
22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro FertilizationAnelisa Gollo Dantas, Adriana Bortolai, Mariana Moysés-Oliveira, et al.
Journal of Applied Genetics|December 19, 2012
Ring chromosome 10: report on two patients and review of the literatureRoberta Santos Guilherme, Chong Ae Kim, Luis Garcia Alonso, et al.
Molecular Cytogenetics|May 14, 2015
Terminal 18q deletions are stabilized by neotelomeresRoberta Santos Guilherme, Karen E Hermetz, Patrícia Teixeira Varela, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Deletion 22q11.2: report of a complex meiotic mechanism of originSintia Iole Nogueira, April M Hacker, Fernanda T S Bellucco, et al.
American Journal of Medical Genetics|November 20, 2002
Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequenceJuliana Godoy Assumpção, Windy Berkofsky-Fessler, Nilma Viguetti Campos, et al.
Journal of Molecular Histology|November 24, 2011
Cytogenetic instability of dental pulp stem cell linesMonica Talarico Duailibi, Leslie Domenici Kulikowski, Silvio Eduardo Duailibi, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|October 19, 2012
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?Roberta Santos Guilherme, Elisabeth Klein, Claudia Venner, et al.
Human Genetics|December 17, 2015
Incorporation of 5-ethynyl-2'-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangementsLuiza Sisdelli, Angela Cristina Vidi, Mariana Moysés-Oliveira, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 23, 2012
Autistic disorder phenotype associated to a complex 15q intrachromosomal rearrangementDenise Maria Christofolini, Vera Ayres Meloni, Marco Antonio de Paula Ramos, et al.
Pageof 9