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Oftalmologia (Bucharest, Romania : 1990)|January 1, 1997
[Familial congenital aniridia]I Zolog, V Belengeanu, S Marinca, et al.Advances in Medical Sciences|June 27, 2009
Ichthyosis congenita, harlequin fetus type: a case reportV Belengeanu, D Stoicanescu, M Stoian, et al.Clinical Genetics|June 1, 1993
Distal arthrogryposis with autosomal dominant inheritance and reduced penetrance in females: the Gordon syndromeD M Ioan, V Belengeanu, C Maximilian, et al.Endocrinologie|July 1, 1988
Leprechaunism: report of two cases and reviewD Ioan, L Dumitriu, V Belengeanu, et al.Endocrinologie|January 1, 1986
Trisomy 8 syndrome. A report of 2 casesD Ioan, L Dumitriu, P Muşeţeanu, et al.Endocrinologie|April 1, 1985
47,XXX/48,XXXX in a retarded three year old girl with multiple somatic anomaliesD Ioan, N Hîrşovescu, L Dumitriu, et al.Genetic Counseling (Geneva, Switzerland)|August 6, 2005
Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?V Belengeanu, K Rozsnyai, S Farcaş, et al.Balkan Journal of Medical Genetics : BJMG|August 14, 2023
Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young TeenagerD E Popescu, D Marian, M Zeleniuc, et al.Endocrinologie|October 1, 1985
Partial 9p monosomy--a case with hypothyroidismD Ioan, L Dumitriu, P Muşeţeanu, et al.Endocrinologie|January 1, 1987
Extra-small marker chromosomes in couples with reproductive failureD Ioan, L Dumitriu, D Ghergar, et al.Pageof 2