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Human Molecular Genetics|March 7, 2001
WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor networkS Cairo, G Merla, F Urbinati, et al.
Journal of Medical Genetics|December 14, 2004
Detection of aneuploidies by paralogous sequence quantificationS Deutsch, U Choudhury, G Merla, et al.
Oncogene|August 5, 2000
Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?G Meroni, S Cairo, G Merla, et al.
Molecular Syndromology|May 9, 2013
Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel MLL2 MutationI Ratbi, N Fejjal, L Micale, et al.
Molecular Syndromology|May 9, 2013
A 1.3-mb 7q11.23 atypical deletion identified in a cohort of patients with williams-beuren syndromeL M Delgado, M Gutierrez, B Augello, et al.
Oncogene|December 22, 1999
Evidence for interaction between human PRUNE and nm23-H1 NDPKinaseA Reymond, S Volorio, G Merla, et al.
Genetic Counseling (Geneva, Switzerland)|December 3, 2015
MYOCLONIC ASTATIC EPILEPSY IN A PATIENT WITH A DE NOVO 4q21.22q21.23 MICRODUPLICATIONV Ottaviani, A Bartocci, M Pantaleo, et al.
Clinical Genetics|January 26, 2018
Intellectual developmental disorder with cardiac arrhythmia syndrome in a child with compound heterozygous GNB5 variantsH Vernon, J Cohen, P De Nittis, et al.
British Journal of Cancer|November 14, 2014
MicroRNA expression profiling in male and female familial breast cancerR Pinto, S De Summa, K Danza, et al.
Stroke|February 24, 1998
Prevalence of apolipoprotein E alleles in healthy subjects and survivors of ischemic stroke: an Italian Case-Control StudyM Margaglione, D Seripa, C Gravina, et al.
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