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Cancer Genetics|April 9, 2022
t(10;12)(q24;q15): A new cytogenetic marker in hematological malignanciesMarta Bernués, Teresa González, Luis Antonio Corchete, et al.
BMC Genetics|May 28, 2013
Genome-wide linkage analysis of congenital heart defects using MOD score analysis identifies two novel lociAntònia Flaquer, Clemens Baumbach, Estefania Piñero, et al.
Medicina Clinica|February 25, 2017
Recommendations for the use of microarrays in prenatal diagnosisJavier Suela, Isabel López-Expósito, María Eugenia Querejeta, et al.
Bioconjugate Chemistry|July 19, 2022
Role of Common Cell Culture Media Supplements on Citrate-Stabilized Gold Nanoparticle Protein Corona Formation, Aggregation State, and the Consequent Impact on Cellular UptakeFrancesco Barbero, Sara Michelini, Oscar H Moriones, et al.
Molecular Vision|January 11, 2013
Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3Gema García-García, María J Aparisi, Regina Rodrigo, et al.
Neuromuscular Disorders : NMD|September 2, 2006
Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1)William Wallefeld, Sabine Krause, Kristen J Nowak, et al.
Genes|May 28, 2022
New Variant in Placophilin-2 Gene Causing Arrhythmogenic MyocardiopathyFiama Caimi-Martinez, Guido Antoniutti, Rocio Blanco, et al.
Plos One|October 3, 2012
Birds of a feather: Neanderthal exploitation of raptors and corvidsClive Finlayson, Kimberly Brown, Ruth Blasco, et al.
European Journal of Human Genetics : EJHG|March 23, 2007
Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardationLaura Torres-Juan, Jordi Rosell, Montse Morla, et al.
International Journal of Cardiology|June 15, 2010
The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humansTomás Ripoll Vera, Lorenzo Monserrat Iglesias, Manuel Hermida Prieto, et al.
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