Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature

Por Dasouki, Majed J, Youngs, Erin L, Hovanes, Karine
Publicado em 2011

PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication

Por Dawson, Angelika J., Cox, Janice, Hovanes, Karine, Spriggs, Elizabeth
Publicado no Case Rep Genet (2015)

The 3q29 Microdeletion Syndrome: Report of Three New Unrelated Patients and In Silico “RNA Binding” Analysis of the 3q29 Region

Por Dasouki, Majed J., Lushington, Gerald H., Hovanes, Karine, Casey, James, Gorre, Mereceds
Publicado em 2011

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders or Learning Disability Presenting for Genetic Services

Por Roberts, Jennifer L., Hovanes, Karine, Dasouki, Majed, Manzardo, Ann M., Butler, Merlin G.
Publicado no Gene (2013)

Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype

Por Paloneva, Juha, Manninen, Tuula, Christman, Grant, Hovanes, Karine, Mandelin, Jami, Adolfsson, Rolf, Bianchin, Marino, Bird, Thomas, Miranda, Roxana, Salmaggi, Andrea, Tranebjærg, Lisbeth, Konttinen, Yrjö, Peltonen, Leena
Publicado em 2002