A COMPARATIVE STUDY OF THE CHROMOSOME BANDING PATTERNS OF MESOCRICETUS NEWTONI AND MESOCRICETUS AURATUS = ETUDE COMPARATIVE DES DISPOSITIONS DES BANDES DES CHROMOSOMES DES HAMSTERS M. N. ET M. A.VOICULESCU I.1974; Z. SAUGETIERKDE; DTSCH.; DA. 1974; VOL. 39; NO 4; PP. 211-219; ABS. ALLEM.; BIBL. 18REF.Article

HETEROCHROMATIN (C-BANDS) IN SOMATIC AND MALE GERM CELLS IN THREE SPECIES OF MICROTINAEZENZES MT; VOICULESCU I.1975; GENETICA; PAYS-BAS; DA. 1975; VOL. 45; NO 2; PP. 263-272; BIBL. 15 REF.Article

C-BANDING PATTERNS IN SALMO TRUTTA, A SPECIES OF TETRAPLOID ORIGIN = TYPES DE BANDES C CHEZ S. T., UNE ESPECE D'ORIGINE TETRAPLOIDEZENKES MT; VOICULESCU I.1975; GENETICA; PAYS-BAS; DA. 1975; VOL. 45; NO 4; PP. 531-536; BIBL. 14 REF.Article

KARYOTYP UND HETEROCHROMATINMUSTER DES RUMAENISCHEN HAMSTERS (MESOCRICETUS NEWTONI) = CARYOTYPE ET TYPE D'HETEROCHROMATINE CHEZ LE HAMSTER ROUMAIN (M. N.)VOICULESCU I; VOGEL W; WOLF U et al.1972; CHROMOSOMA; ALLEM.; DA. 1972; VOL. 39; NO 2; PP. 215-224; ABS. ANGL.; BIBL. 18 REF.Serial Issue

On the development of a standard two-dimensional polypeptide map of the human X chromosomeMULLER, U; VOICULESCU, I.Human genetics. 1984, Vol 67, Num 4, pp 400-405, issn 0340-6717Article

CYTOGENETIC AND BIOCHEMICAL DIFFERENCES BETWEEN APODEMUS SYLVATICUS AND APODEMUS FLAVICOLLIS, POSSIBLY RESPONSIBLE FOR THE FAILURE TO INTERBREED = DIFFERENCES CYTOGENETIQUES ET BIOCHIMIQUES ENTRE A. S. ET A. F. VRAISEMBLABLEMENT RESPONSABLES DE L'ABSENCE DE CROISEMENTENGEL W; VOGEL W; VOICULESCU I et al.1973; COMP. BIOCHEM. PHYSIOL. B; G.B.; DA. 1973; VOL. 44; NO 4; PP. 1165-1173; H.T. 2; BIBL. 2P.Serial Issue

On-Chip Hotplate for Temperature Control of CMOS SAW ResonatorsNORDIN, A. N; VOICULESCU, I; ZAGHLOUL, M et al.Symposium on design, test, integration and packaging of MEMS-MOEMS. 2008, pp 71-76, isbn 978-2-35500-006-5, 1Vol, 6 p.Conference Paper

Deletion 11q23.3 without familial predispositionHAUSMANN, C; BACK, E; WOLFF, G et al.Human genetics. 1988, Vol 80, Num 2, issn 0340-6717, 205Article

De novo isochromosome 18p in two patients : cytogenetic diagnosis and confirmation by chromosome paintingBACK, E; TODER, R; VOICULESCU, I et al.Clinical genetics. 1994, Vol 45, Num 6, pp 301-304, issn 0009-9163Article

A retrospective CISS hybridization analysis of a case with de novo translocation t (18;22) resulting in an 18p - syndromeVOICULESCU, I; TODER, R; BACK, E et al.Clinical genetics. 1993, Vol 43, Num 6, pp 318-320, issn 0009-9163Article

Trisomy 22 in a newborn with multiple malformationsVOICULESCU, I; BACK, E; DUNCAN, A. M. V et al.Human genetics. 1987, Vol 76, Num 3, pp 298-301, issn 0340-6717Article

A putative gene family in 15q-13 and 16p11.2 : possible implications for Prader-Willi and Angelman syndromesBUITING, K; GREGER, V; BROWNSTEIN, B. H et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 12, pp 5457-5461, issn 0027-8424Article