Helena G. Ilyina

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

Dieter Kotzot, Silke Schmitt, Fabiana Bernasconi et al. · Human Molecular Genetics · 1995 · 302 citations · Full text

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

Diane Beysen, Jeroen Raes, Bart P. Leroy et al. · The American Journal of Human Genetics · 2005 · 115 citations · Full text

Blepharophimosis Syndrome, Autoimmune Disease, Novel Disease-causing Mechanism +9

SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype

Elke Botzenhart, Andrew Green, Helena G. Ilyina et al. · Human Mutation · 2005 · 68 citations

Maternal uniparental disomy 7 - review and further delineation of the phenotype

Dieter Kotzot, Damina Balmer, Alessandra Baumer et al. · European Journal of Pediatrics · 2000 · 66 citations

Infertility, Fertility, Genetics +11

Gollop-Wolfgang complex in a 3-month-old girl

Iosif W. Lurie, Helena G. Ilyina, John M. Opitz et al. · American Journal of Medical Genetics · 1986 · 26 citations

Developmental Anomaly, Child Psychology, Early Childhood Development +5