HUMAN X CHROMOSOMES: SYNCHRONY OF DNA REPLICATION IN DIPLOID AND TRIPLOID FIBROBLASTS WITH MULTIPLE ACTIVE OR INACTIVE X CHROMOSOMESWILLARD HF; BREG WR.1980; SOMAT. CELL GENET.; USA; DA. 1980; VOL. 6; NO 2; PP. 187-198; BIBL. 46 REF.Article

AUTOSOMAL CHROMOSOME DISORDERS AND VARIATIONS = TROUBLES CHROMOSOMIQUES AUTOSOMIQUESMILLER OJ; BREG WR.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 294; NO 11; PP. 596-598; BIBL. 4 REF.Article

A CASE OF PARTIAL 14 TRISOMY 47,XY, (14Q-)+ AND TRANSLOCATION T (9P+; 14Q-) IN MOTHER AND BROTHER = UN CAS DE TRISOMIE 14 PARTIELLE 47, XY, (14Q-)+ AVEC TRANSLOCATION T (9P+; 14Q-) CHEZ LA MERE ET LE FRERESHORT EM; SOLITAIRE GB; BREG WR et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 367-373; BIBL. 16 REF.Serial Issue

INCREASED FREQUENCY OF HETEROZYGOTES FOR ALPHA ₁ ANTITRYPSIN VARIANTS IN INDIVIDUALS WITH EITHER SEX CHROMOSOME MOSAICISM OR TRISOMY 21 = AUGMENTATION DE LA FREQUENCE DES HETEROZYGOTES POUR LES VARIANTS DE L'ALPHA ₁-ANTITRYPSINE CHEZ LES INDIVIDUS PRESENTANT SOIT UNE MOSAICITE DES CHROMOSOMES SEXUELS SOIT UNE TRISOMIE 21FINEMAN RM; KIDD KK; JOHNSON AM et al.1976; NATURE; G.B.; DA. 1976; VOL. 260; NO 5549; PP. 320-321; BIBL. 6 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME 4 FROM A SUBJECT WITH WOLF'S SYNDROME. REPOSITORY IDENTIFICATION NO.6M-72.BREG WR; ARONSON MM; GREENE AE et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 5; PP. 307-308; BIBL. 5 REF.Article

DELETION IN THE SHORT ARM OF CHROMOSOME 9 FROM A SUBJECT WITH CONGENITAL CEREBRAL MALDEVELOPMENT. REPOSITORY IDENTIFICATION NO. GM-870.BREG WR; ARONSON MM; HILL R et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 5; PP. 296-297; BIBL. 1 REF.Article

EVIDENCE FOR METHYLATION OF INACTIVE HUMAN RRNA GENES IN AMPLIFIED REGIONSUMADEVI TANTRAVAHI; BREG WR; WERTELECKI V et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 315-320; BIBL. 40 REF.Article

MULTIPLE CONGENITAL ANOMALIES-MENTAL RETARDATION (MCA/MR) SYNDROME DUE TO PARTIAL 1Q DUPLICATION AND POSSIBLE 18P DELECTION: A STUDY OF FOUR INDIVIDUALS IN TWO FAMILIESLIBERFARB RM; BREG WR; ATKINS L et al.1979; AMER. J. MED. GENET.; USA; DA. 1979; VOL. 4; NO 1; PP. 27-37; BIBL. 13 REF.Article

CHROMOSOME 3 DUPLICATION QDELETION P SYNDROME.FINEMAN RM; HECHT F; ABLOW RC et al.1978; PEDIATRICS; U.S.A.; DA. 1978; VOL. 61; NO 4; PP. 611-618; BIBL. 8 REF.Article

CHROMOSOMAL ABNORMALITY (46, XX, 3P+) IN A CASE OF THE MECKEL SYNDROME.HSIA YE; VANITHA APPADORAI; BREG WR et al.1974; BIRTH DEFECTS ORIGIN SER.; U.S.A.; DA. 1974; VOL. 10; NO 8; PP. 19-25; BIBL. 9 REF.Article

PRESENCE OF H-Y ANTIGEN IN PATIENTS WITH ULLRICH-TURNER SYNDROME AND X-CHROMOSOME REARRANGEMENTSHASELTINE FP; DE PONTE KK; BREG WR et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 1; PP. 97-107; BIBL. 1 P.Article

H-Y ANTIGEN NEGATIVE PATIENTS WITH TESTICULAR TISSUE AND 46, XY KARYOTYPEHASELTINE FP; GENEL M; CRAWFORD JD et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 3; PP. 265-268; BIBL. 22 REF.Article

REGULATION OF RRNA GENE EXPRESSION IN A HUMAN FAMILIAL 14P+ MARKER CHROMOSOMEMILLER DA; BREG WR; WARBURTON D et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 3; PP. 289-297; BIBL. 22 REF.Article

RETINOBLOSTOMA AND CHROMOSOME ABNORMALITY. PARTIAL DELETION OF THE LONG ARM OF CHROMOSOME 13 = RETINOBLASTOME ET ANOMALIE CHROMOSOMIQUE. DELETION PARTIELLE DU BRAS LONG DU CHROMOSOME 13HOWARD RO; BREG WR; ALBERT DM et al.1975; ARCH. OPHTHALMOL.; U.S.A.; DA. 1975; VOL. 92; NO 6; PP. 490-493; BIBL. 21 REF.Article

ANGIOIMMUNOBLASTIC LYMPHADENOPATHY, EVOLUTION TO A BURKITT-LIKE LYMPHOMAMAZUR EM; LOVETT DH; ENRIQUEZ RE et al.1979; AMER. J. MED.; USA; DA. 1979; VOL. 67; NO 2; PP. 317-324; BIBL. 44 REF.Article

H-Y ANTIGEN EXPRESSION IN PATIENTS WITH X-AUTOSOMAL TRANSLOCATIONS AND GONADAL DYSGENESISHASELTINE FP; LYNCH VA; VAN DYKE DL et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 13; NO 2; PP. 115-123; BIBL. 26 REF.Article

THE INTERREGIONAL CYTOGENETIC RESISTER SYSTEM (ICRS)PRESCOTT GH; RIVAS MI; SHANBECK L et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 269-279; BIBL. 6 REF.Article

MAPPING THE LOCUS OF THE H-Y GENE ON THE HUMAN Y CHROMOSOME.KOO GC; WACHTEL SS; KRUPEN BROWN K et al.1977; SCIENCE; U.S.A.; DA. 1977; VOL. 198; NO 4320; PP. 940-942; BIBL. 17 REF.Article