Results for
""Chromosomes""[mesh_terms]

Balanced translocations in mental retardation.

R Frank Kooy, Geert Vandeweyer

Human genetics 2009;126(1):133-47

Additional chromosomal abnormalities in patients with acute promyelocytic leukaemia (APL) do not confer poor prognosis: results of APL 93 trial.

S De Botton, S Chevret, M Sanz, H Dombret, X Thomas, A Guerci, M Fey, C Rayon, F Huguet, J J Sotto, C Gardin, P Cony Makhoul, P Travade, E Solary, N Fegueux, D Bordessoule, J San Miguel, H Link, B Desablens, A Stamatoullas, E Deconinck, K Geiser, U Hess, F Maloisel, S Castaigne, C Preudhomme, C Chomienne, L Degos, P Fenaux

British journal of haematology 2001;111(3):801-6

Evidence for defective retinoid transport and function in late onset Alzheimer's disease.

Ann B Goodman, Arthur B Pardee

Proceedings of the National Academy of Sciences of the United States of America 2003;100(5):2901-5

Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review.

Merlin G Butler

International journal of molecular sciences 2023;24(5):4271

Plant contributions to our understanding of sex chromosome evolution.

Deborah Charlesworth

The New phytologist 2016;208(1):52-65

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

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

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

Guideline recommendations for diagnosis and clinical management of Ring14 syndrome-first report of an ad hoc task force.

Berardo Rinaldi, Alessandro Vaisfeld, Sergio Amarri, Chiara Baldo, Giuseppe Gobbi, Pamela Magini, Erto Melli, Giovanni Neri, Francesca Novara, Tommaso Pippucci, Romana Rizzi, Annarosa Soresina, Laura Zampini, Orsetta Zuffardi, Marco Crimi

Orphanet journal of rare diseases 2018;12(1):69

A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.

Jie Hu, Sofia Shekhter-Levin, Peter H Shaw, Carolyn Bay, Sally Kochmar, Urvashi Surti

Cancer genetics and cytogenetics 2005;156(1):62-7

Aneuploidy, inflammation and diseases.

Micheline Kirsch-Volders, Michael Fenech

Mutation research 2022;824():111777

Signaling revisited in acute promyelocytic leukemia.

P G Lutz, C Moog-Lutz, Y E Cayre

Leukemia 2002;16(10):1933-9

Epilepsy in ring 14 chromosome syndrome.

Nicola Specchio, Marina Trivisano, Domenico Serino, Simona Cappelletti, Antonio Carotenuto, Dianela Claps, Carlo Efisio Marras, Lucia Fusco, Maurizio Elia, Federico Vigevano

Epilepsy & behavior : E&B 2013;25(4):585-92

Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci.

Matthias Munz, Gesa M Richter, Bruno G Loos, Søren Jepsen, Kimon Divaris, Steven Offenbacher, Alexander Teumer, Birte Holtfreter, Thomas Kocher, Corinna Bruckmann, Yvonne Jockel-Schneider, Christian Graetz, Ilyas Ahmad, Ingmar Staufenbiel, Nathalie van der Velde, André G Uitterlinden, Lisette C P G M de Groot, Jürgen Wellmann, Klaus Berger, Bastian Krone, Per Hoffmann, Matthias Laudes, Wolfgang Lieb, Andre Franke, Jeanette Erdmann, Henrik Dommisch, Arne S Schaefer

European journal of human genetics : EJHG 2019;27(1):102-113

Chasing the cancer demon.

A G Knudson

Annual review of genetics 2001;34():1-19

Acute promyelocytic leukemia with complex translocation t(5;17;15)(q35;q21;q22): case report and review of the literature.

Sung Ran Cho, Seo-Jin Park, Hyon J Kim, Il Joong Park, Jong Rak Choi, Hyun Joo Jung, Jun Eun Park

Journal of pediatric hematology/oncology 2012;33(7):e326-9