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Cancer Genetics and Cytogenetics|June 20, 2002
Spectrum of genetic changes in gastro-esophageal cancer cell lines determined by an integrated molecular cytogenetic approachCarla Rosenberg, Eric Geelen, Marije J IJszenga, et al.
Human Genetics|February 24, 2005
Array CGH detection of a cryptic deletion in a complex chromosome rearrangementCarla Rosenberg, Jeroen Knijnenburg, Maria de Lourdes Chauffaille, et al.
American Journal of Medical Genetics. Part A|September 5, 2003
Multiple supernumerary ring chromosomes of different origin in a patient: a clinical report and review of the literatureGeoff C Beverstock, Vladimir Bezrookove, Paul Mollevanger, et al.
European Journal of Human Genetics : EJHG|April 23, 2015
Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autismCamila Oliveira Freitas Machado, Karina Griesi-Oliveira, Carla Rosenberg, et al.
Cancer Genetics and Cytogenetics|April 25, 2006
Genomic array and expression analysis of frequent high-level amplifications in adenocarcinomas of the gastro-esophageal junctionHerman van Dekken, Kees Vissers, Hugo W Tilanus, et al.
Meta Gene|January 22, 2015
Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH geneNatália D Linhares, Marta Svartman, Mauro Ivan Salgado, et al.
American Journal of Medical Genetics. Part A|November 5, 2022
SCAF4-related syndromic intellectual disabilityLaura Machado Lara Carvalho, Carla Franchi Pinto, Marília de Oliveira Scliar, et al.
Cancer Genetics and Cytogenetics|April 24, 2004
A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B geneVladimir Bezrookove, Shama L van Zelderen-Bhola, Antoinette Brink, et al.
Obesity Research & Clinical Practice|February 24, 2021
A novel MYT1L mutation in a boy with syndromic obesity: Case report and literature reviewLaura M L Carvalho, Carla S D'Angelo, Zan Mustacchi, et al.
Genetics and Molecular Biology|January 4, 2014
Germline DNA copy number variation in individuals with Argyrophilic grain disease reveals CTNS as a plausible candidate geneDarine Villela, Lilian Kimura, David Schlesinger, et al.
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