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Results for
""Chromosomes, Human, Pair 21""[mesh_terms]

17 Results

Searching titles within these results

Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.

Federico Vigevano, Lucia Fusco, Matteo Di Capua, Rossella Capolino, Cristina Digilio, Simona Cappelletti, Marina Trivisano, Antonio Carotenuto, Nicola Specchio

American journal of medical genetics. Part A 2011;155A(4):911-4

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Down syndrome--genetic and nutritional aspects of accompanying disorders.

Joanna Wyka, Dominika Mazurek

Roczniki Panstwowego Zakladu Higieny 2016;66(3):189-94

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A novel c132-134del mutation in Unverricht-Lundborg disease and the review of literature of heterozygous compound patients.

Vincenzo Di Lazzaro, Giovanni Di Pino, Federica Assenza, Chiara Campana, Mario Tombini, Elena Gennaro, Antonella Benvenga, Giovanni Assenza

Epilepsia 2017;58(2):e31-e35

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An infant with Down syndrome and retinoblastoma. A possible non-fortuitous association.

P Gembara, F Demeocq, M Vekemans, L Desjardins, C Francannet, A J Sasco, D Satgé

Ophthalmic genetics 2001;22(2):117-23

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Granulocyte colony-stimulating factor and leukemogenesis.

Lorena Lobo de Figueiredo, Rodrigo Siqueira de Abreu e Lima, Eduardo Magalhães Rego

Mediators of inflammation 2005;13(3):145-50

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Down syndrome, drug metabolism and chromosome 21.

Yubin Ge, Jeffrey W Taub

Pediatric blood & cancer 2005;44(1):33-9

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Pattern of malignant disorders in individuals with Down's syndrome.

H Hasle

The Lancet. Oncology 2002;2(7):429-36

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TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness.

Michel Guipponi, Hamish Steele Scott, Stylianos Emmanuel Antonarakis

Frontiers in bioscience : a journal and virtual library 2007;13():1557-67

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Down's Syndrome and Triple Negative Breast Cancer: A Rare Occurrence of Distinctive Clinical Relationship.

Brian Leyland-Jones, Pradip De, Casey Williams, Yuliang Sun, Rachel Elsey, Amanda McMillan, Kirstin Williams, Jessica Klein, Amy Krie, Nandini Dey

International journal of molecular sciences 2018;18(6):1218

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Susceptibility to aneuploidy in young mothers of Down syndrome children.

Lucia Migliore, Francesca Migheli, Fabio Coppedè

TheScientificWorldJournal 2009;9():1052-60

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The transcriptome profile of human trisomy 21 blood cells.

Francesca Antonaros, Rossella Zenatelli, Giulia Guerri, Matteo Bertelli, Chiara Locatelli, Beatrice Vione, Francesca Catapano, Alice Gori, Lorenza Vitale, Maria Chiara Pelleri, Giuseppe Ramacieri, Guido Cocchi, Pierluigi Strippoli, Maria Caracausi, Allison Piovesan

Human genomics 2022;15(1):25

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Complex rearrangement of chromosomes 19, 21, and 22 in Ewing sarcoma involving a novel reciprocal inversion-insertion mechanism of EWS-ERG fusion gene formation: a case analysis and literature review.

Georges Maire, Christopher W Brown, Jane Bayani, Carlos Pereira, Denis H Gravel, John C Bell, Maria Zielenska, Jeremy A Squire

Cancer genetics and cytogenetics 2008;181(2):81-92

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The association of reduced folate carrier 80G>A polymorphism to outcome in childhood acute lymphoblastic leukemia interacts with chromosome 21 copy number.

Jannie Gregers, Ib Jarle Christensen, Kim Dalhoff, Birgitte Lausen, Henrik Schroeder, Steen Rosthoej, Niels Carlsen, Kjeld Schmiegelow, Curt Peterson

Blood 2010;115(23):4671-7

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NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome.

Antonella Izzo, Anna Conti, Paolo Pinton, Mariastella Zannini, Rosella Scrima, Rita Cicatiello, Simone Patergnani, Tiziana De Cristofaro, Gaetano Calì, Ferdinando Bonfiglio, Rosanna Manco, Lucio Nitsch

Human molecular genetics 2016;23(16):4406-19

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New mechanisms of AML1 gene alteration in hematological malignancies.

C Roumier, P Fenaux, M Lafage, M Imbert, V Eclache, C Preudhomme

Leukemia 2003;17(1):9-16

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Results: 1 – 15 / 17

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Results for ""Chromosomes, Human, Pair 21""[mesh_terms]

Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.

Down syndrome--genetic and nutritional aspects of accompanying disorders.

A novel c132-134del mutation in Unverricht-Lundborg disease and the review of literature of heterozygous compound patients.

An infant with Down syndrome and retinoblastoma. A possible non-fortuitous association.

Granulocyte colony-stimulating factor and leukemogenesis.

Down syndrome, drug metabolism and chromosome 21.

Pattern of malignant disorders in individuals with Down's syndrome.

TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness.

Down's Syndrome and Triple Negative Breast Cancer: A Rare Occurrence of Distinctive Clinical Relationship.

Susceptibility to aneuploidy in young mothers of Down syndrome children.

The transcriptome profile of human trisomy 21 blood cells.

Complex rearrangement of chromosomes 19, 21, and 22 in Ewing sarcoma involving a novel reciprocal inversion-insertion mechanism of EWS-ERG fusion gene formation: a case analysis and literature review.

The association of reduced folate carrier 80G>A polymorphism to outcome in childhood acute lymphoblastic leukemia interacts with chromosome 21 copy number.

NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome.

New mechanisms of AML1 gene alteration in hematological malignancies.

Results for
""Chromosomes, Human, Pair 21""[mesh_terms]