RELATIVE ACTIVATION AND INACTIVATION PHENOMENA BETWEEN HOMOLOGOUS AND NONHOMOLOGOUS NUCLEOLUS ORGANIZERS ON THE NORMAL HUMAN G CHROMOSOMESORYE E.1974; CYTOGENET. CELL GENET; SWITZ.; DA. 1974; VOL. 13; NO 14; PP. 352-368; BIBL. 1 P. 1/2Article

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CLONAL KARYOTYPE EVOLUTION IN SOLID TUMOURS IN CHILDREN = EVOLUTION CLONALE DU CARYOTYPE DANS LES TUMEURS SOLIDES CHEZ LES ENFANTSORYE E; DELBEKE MJ.1974; ONCOLOGY; SWITZ.; DA. 1974; VOL. 29; NO 6; PP. 520-533; BIBL. 10 REF.Article

AT (21Q21Q) RING CHROMOSOME = UN CHROMOSOME ANNULAIRE T (21Q21Q)ORYE E; CRAEN M.1974; HUM. HERED.; SWITZ.; DA. 1974; VOL. 24; NO 3; PP. 253-258; BIBL. 12 REF.Article

PARTIAL LONG-ARM DELETION OF CHROMOSOME 8 (PTER->913: 922->9TER) WITHOUT LANYER-OIDION SYNDROMEORYE E; CRAEN M.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 44-46; ABS. FRE; BIBL. 8 REF.Article

SHORT ARM DELETION OF CHROMOSOME 12. REPORT OF TWO NEW CASES. = DELETION DU BRAS COURT DU CHROMOSOME 12. RAPPORT DE DEUX CASORYE E; CRAEN M.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 4; PP. 335-342; BIBL. 8 REF.Article

A PECULIAR T(21;14) TRANSLOCATION, ASSOCIATED WITH A PERICENTRIC INVERSION OF THE Y CHROMOSOME IN A MONGOL BOYORYE E; VERHAAREN H.1974; SEM. HOP., ANN. GENET.; FR.; DA. 1974; VOL. 17; NO 3; PP. 217-220; ABS. FR.; BIBL. 18 REF.Article

COMPLEX CHROMOSOMAL REARRANGEMENT: (YP+; 49-) TRANSLOCATION AND RING CHROMOSOME OF THE 49-CHROMOSOMEORYE E; CRAEN M.1983; ANNALES DE GENETIQUE; ISSN 0003-3995; FRA; DA. 1983; VOL. 26; NO 1; PP. 47-49; ABS. FRE; BIBL. 8 REF.Article

UNEXPECTED FINDINGS WITH THE NEW CHROMOSOME BANDING TECHNIQUES IN A PATIENT FORMERLY DIAGNOSED AS HAVING G-DELETION SYNDROME = RESULTATS INATTENDUS OBTENUS GRACE AUX NOUVELLES TECHNIQUES DE BANDES CHEZ UNE PATIENTE DIAGNOSTIQUEE INITIALEMENT COMME ATTEINTE DE SYNDROME II DE DELETION GORYE E; CRAEN M.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 75-82; ABS. ITAL. FR. ALLEM.; BIBL. 14 REF.Article

PARACENTRIC INVERSIONS: TWO NEW FAMILIAL CASES, INV (7)(Q22Q11) AND INV (11)(Q23Q13)ORYE E; VAN BEVER H.1983; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1983; VOL. 20; NO 3; PP. 231; BIBL. 2 REF.Article

RETINOBLASTOMA AND LONG ARM DELETION OF CHROMOSOME 13. ATTEMPTS TO DEFINE THE DELETED SEGMENT = RETINOBLASTOME ET DELETION DU BRAS LONG DU CHROMOSOME 13. ESSAIS DE DEFINITION DU SEGMENT EN DELETIONORYE E; DELBEKE MJ; VANDENABEELE B et al.1974; CLIN. GENET.; DANM.; DA. 1974; VOL. 5; NO 5; PP. 457-464; BIBL. 14REF.Article

De novo distal trisomy 17qORYE, E; VAN BEVER, H.Annales de génétique (Paris). 1985, Vol 28, Num 1, pp 61-62, issn 0003-3995Article

Trisomy 3p syndrome: report of a new case, due to a chromosomal insertionORYE, E; LAUREYS, G.Annales de génétique (Paris). 1984, Vol 27, Num 4, pp 245-247, issn 0003-3995Article

A 46,XX,10Q+ CHROMOSOME CONSTITUTION IN A GIRL. PARTIAL LONG ARM DUPLICATION OR INSERTIONAL TRANSLOCATION. = CONSTITUTION CHROMOSOMIQUE 46,XX,10Q+ CHEZ UNE FILLE. DUPLICATION PARTIELLE DU BRAS LONG OU TRANSLOCATION AVEC INSERTION.ORYE E; VERHAAREN H; SAMUEL K et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 1; PP. 1-8; BIBL. 8 REF.Article

A NEW CASE OF THE TRISOMY 9P SYNDROME. REPORT OF A PATIENT WITH UNUSUAL CHROMOSOME FINDINGS (46, XX/47, XX, +I (9P)) AND A PECULIAR CONGENITAL HEART DEFECT = UN NOUVEAU CAS DU SYNDROME DE TRISOMIE 9P. OBSERVATION D'UN MALADE AYANT DES CARACTERISTIQUES CHROMOSOMIQUES INHABITUELLES (46, XX/47, XX, +I (9P)) ET UNE CARDIOPATHIE CONGENITALE PARTICULIEREORYE E; VERHAAREN H; VAN EGMOND H et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 7; NO 2; PP. 134-143; BIBL. 22REF.Article

THE 9P-DELETION SYNDROME. REPORT OF A PATIENT WITH A 46,XX,9P-CONSTITUTION DUE TO A PATERNAL T(9P-;15Q+) TRANSLOCATIONORYE E; VERHAAREN H; VAN DEN BOAERT VAN HEESVELDE AM et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 5; PP. 349-357; BIBL. 8 REF.Article

SIGNIFICANCE OF THE SINGLE UMBILICAL ARTERY. A CLINICAL, RADIOLOGICAL, CHROMOSOMAL AND DERMATOGLYPHIC STUDY = SIGNIFICATION DE L'ARTERE OMBILICALE UNIQUE. UNE ETUDE CLINIQUE, RADIOLOGIQUE, CHROMOSOMIQUE ET DERMATOGLYPHIQUEVLIETINCK RF; THIERY M; ORYE E et al.1972; ARCH. DIS. CHILDH; G.B.; DA. 1972; VOL. 47; NO 254; PP. 639-642; BIBL. 30REF.Serial Issue

Distal trisomy 14q due to tandem duplication (q24→q32)ORYE, E; VAN BEVER, H; DESIMPEL, H et al.Annales de génétique (Paris). 1983, Vol 26, Num 4, pp 238-239, issn 0003-3995Article

Mosaic and non-mosaic trisomy 15q2ORYE, E; LAUREYS, G; VERHAAREN, H et al.Annales de génétique (Paris). 1985, Vol 28, Num 1, pp 58-60, issn 0003-3995Article

A NEW, SIMPLE AND RAPID METHOD FOR ENUMERATING HUMAN T LYMPHOCYTES IN FULL BLOOD: THE E. COLI (ATCC 11303) ROSETTE TESTORYE E; BENOIT Y; ROESBEKE L et al.1983; JOURNAL OF IMMUNOLOGICAL METHODS; ISSN 0022-1759; NLD; DA. 1983; VOL. 60; NO 3; PP. 369-377; BIBL. 20 REF.Article

A CASE OF RETINOBLASTOMA, ASSOCIATED WITH HISTIOCYTOSIS-X AND MOSAICISM OF A DELETED D-GROUP CHROMOSOME (13Q14->Q31)ORYE E; BENOIT Y; COPPIETERS R et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 1; PP. 37-39; BIBL. 9 REF.Article

β-Glucuronidase activity in human T and B lymphocytes and the Tυ and Tγ subpopulationsORYE, E; PLUM, J; DE SMEDT, M et al.Histochemistry (Berlin). 1984, Vol 81, Num 3, pp 287-290, issn 0301-5564Article

Complete trisomy 5p owing to de novo translocation t(5;22) (q11:p11) with isochromosome 5p associated with a familial pericentric inversion of chromosome 2, inv 2(p21q11)ORYE, E; BENOIT, Y; VAN MELE, B et al.Journal of medical genetics. 1983, Vol 20, Num 5, pp 394-396, issn 0022-2593Article

Meningeal leukaemia in the blastic phase of chronic granulocytic leukaemiaVAN BEVER, H; BENOIT, Y; DELBEKE, M. J et al.European journal of pediatrics. 1985, Vol 144, Num 4, pp 417-418, issn 0340-6199Article

PENTASOMY 21 CHARACTERIZING SPONTANEOUSLY REGRESSING CONGENITAL ACUTE LEUKEMIA = PENTASOMIE 21 CARACTERISTIQUE D'UNE REGRESSION SPONTANEE DE LA LEUCEMIE AIGUE CONGENITALEVAN DEN BERGHE H; VERMAALEN K; BROECKAERT VAN ORSHOVEN A et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 9; NO 1; PP. 19-23; ABS. ENG; BIBL. 11 REF.; FIGArticle