au.\*:("HOVANES, Karine")
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The 3q29 Microdeletion Syndrome: Report of Three New Unrelated Patients and In Silico RNA Binding Analysts of the 3q29 RegionDASOUKI, Majed J; LUSHINGTON, Gerald H; HOVANES, Karine et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 7, pp 1654-1660, issn 1552-4825, 7 p.Article
β-catenin-sensitive isoforms of lymphoid enhancer factor-1 are selectively expressed in colon cancerHOVANES, Karine; LI, Tony W. H; MUNGUIA, Jesus E et al.Nature genetics. 2001, Vol 28, Num 1, pp 53-57, issn 1061-4036Article
The phenotype of short stature homeobox gene (SHOX) deficiency in childhood : Contrasting children with leri-weill dyschondrosteosis and turner syndromeROSS, Judith L; KOWAL, Karen; QUIGLEY, Charmian A et al.The Journal of pediatrics. 2005, Vol 147, Num 4, pp 499-507, issn 0022-3476, 9 p.Article
Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotypePALONEVA, Juha; MANNINEN, Tuula; TRANEBIAERG, Lisbeth et al.American journal of human genetics. 2002, Vol 71, Num 3, pp 656-662, issn 0002-9297Article
A Novel Familial 11p15.4 Microduplication Associated With Intellectual Disability, Dysmorphic Features, and Obesity With Involvement of the ZNF214 GeneSOFOS, Elvera; PESCOSOLIDO, Matthew F; QUINTOS, Jose B et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 50-58, issn 1552-4825, 9 p.Article