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Publications by Eunice Matoso
Interstitial 287 Kb Deletion of 4p16.3 Including FGFRL1 Gene Associated With Language Impairment and Overgrowth
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Critical Region in 2q31.2q32.3 Deletion Syndrome: Report of Two Phenotypically Distinct Patients, One With an Additional Deletion in Alagille Syndrome Region
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Related publications
Microdeletion of 7p12.1p13, Including IKZF1 , Causes Intellectual Impairment, Overgrowth, and Susceptibility to Leukaemia
British Journal of Haematology
Hematology
Interstitial Deletion of Distal 13q Associated With Hirschsprung's Disease.
Journal of Medical Genetics
Genetics
Obesity and Abnormal Behaviour Associated With Interstitial Deletion of Chromosome 18 (Q12.2q21.1).
Journal of Medical Genetics
Genetics
Distinctive Phenotypic Abnormalities Associated With Submicroscopic 21q22 Deletion Including DYRK1A
Molecular Syndromology
Genetics
Breakpoint Identification, Detection and Frequency of the 65-Kb Deletion in the Cystinosis Gene, CTNS
Pediatric Research
Child Health
Pediatrics
Perinatology
Genetic Syndromes Associated With Overgrowth in Childhood
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
Phenotypic and Genotypic Variability in Four Males With MECP2 Gene Sequence Aberrations Including a Novel Deletion
Pediatric Research
Child Health
Pediatrics
Perinatology
Heterozygous Deletion of the LRFN2 Gene Is Associated With Working Memory Deficits
European Journal of Human Genetics
Genetics
