Tiiu Ilus

Three patients with 9p deletions including DMRT1 and DMRT2: A girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development

Katrin Õunap, Riina Žordania, Liina Kiho et al. · American Journal of Medical Genetics Part A · 2004 · 73 citations

Xy Complement, Cytogenetics, Genetics +19

Variant chromosome 3 (inv3) in normal newborns and their parents, and in children with mental retardation

Aavo‐Valdur Mikelsaar, Tiiu Ilus, Sirje Kivi · Human Genetics · 1978 · 65 citations

Down Syndrome, Variant Chromosome 3, Developmental Anomaly +10

Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented

Eve Õiglane‐Shlik, Tiina Talvik, Riina Žordania et al. · American Journal of Medical Genetics Part A · 2006 · 37 citations

A girl with inverted triplication of chromosome 3q25.3 → q29 and multiple congenital anomalies consistent with 3q duplication syndrome

Katrin Õunap, Tiiu Ilus, Oliver Bartsch · American Journal of Medical Genetics Part A · 2005 · 30 citations

"Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation.

Raik Mikelsaar, Iosif W. Lurie, Tiiu Ilus · Journal of Medical Genetics · 1996 · 25 citations · Full text