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DELETION MAPPING OF THE HUMAN X CHROMOSOME. = CARTE DU CHROMOSOME X HUMAIN D'APRES L'ETUDE DE DELETIONSDE LA CHAPELLE A; SCHRODER J; HAAHTELA T et al.1975; HEREDITAS; SUEDE; DA. 1975; VOL. 80; NO 1; PP. 113-120; BIBL. 22 REF.Article

CONTRIBUTION A L'ETUDE DE L'INACTIVATION D'UN CHROMOSOME X CHEZ LA FEMMEGILGENKRANTZ S; ALEXANDRE P; SABORIO M et al.1974; C.R. SOC. BIOL.; FR.; DA. 1974; VOL. 168; NO 8-9; PP. 1063-1067; ABS. ANGL.; BIBL. 18 REF.Article

PREMATURE CENTROMERE DIVISION: A MECHANISM OF NON-DISJUNCTION CAUSING X CHROMOSOME ANEUPLOIDY IN SOMATIC CELLS OF MAN = LA DIVISION PREMATUREE DU CENTROMERE, UN MECANISME DE NON-DISJONCTION CAUSE D'ANEUPLOIDIE DU CHROMOSOME X DANS LES CELLULES SOMATIQUES HUMAINESFITZGERALD FH; PICKERING AF; MERCER JM et al.1975; ANN. HUM. GENET.; G.B.; DA. 1975; VOL. 38; NO 4; PP. 417-428; BIBL. 7 REF.Article

CHROMOSOME X ET REPLICATION TARDIVE. ESSAI D'INTERPRETATION A L'AIDE DE CAS PATHOLOGIQUES ET DES TECHNIQUES CYTOGENETIQUES AVEC AUTORADIOGRAPHIE ET B.U.D.R.GILGENKRANTZ S; ALEXANDRE P; BAUE G et al.1975; LYON MED.; FR.; DA. 1975; VOL. 233; NO 3; PP. 231-240; ABS. ANGL.; BIBL. 1P.1/2Article

ANOMALIES DE STRUCTURE DU CHROMOSOME X CHEZ LES SUJETS DE PHENOTYPE FEMININDEVIN CATHERINE.sd; FRA; DA. S.D.; 118; 135-VII P.-PL.; 30 CM; BIBL. 91 REF.; TH.: MED./NANCY 1/1979Thesis

X chromosome inactivation: theme and variationsMIGEON, B. R.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 8-16, issn 1424-8581, 9 p.Article

ICF syndrome cells as a model system for studying X chromosome inactivationGARTLER, S. M; HANSEN, R. S.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 25-29, issn 1424-8581, 5 p.Article

REPLICATION AND INACTIVATION OF A DICENTRIC X FORMED BY TELOMERIC FUSIONSARTO GE; THERMAN E.1980; AMER. J. OBSTETR. GYNECOL.; USA; DA. 1980; VOL. 136; NO 7; PP. 904-911; BIBL. DISSEM.Article

CYTOLOGICAL FINDINGS OF 10 CASES WITH I(XQ) AND ONE WITH DIC(X) (QTER->CEN->P22::P11->QTER).FUJITA H; TANIGAWA Y; YOSHIDA Y et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 2; PP. 147-155; BIBL. 18 REF.Article

A FAMILIAL X-22 TRANSLOCATION WITH AN EXTRA X CHROMOSOME = UNE TRANSLOCATION FAMILIALE X-22 AVEC UN EXTRA-CHROMOSOME XJENKINS MB; DAVIS E; THELEN TH et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 26; NO 6; PP. 736-745; BIBL. 18REF.Article

CHROMOSOME MEASUREMENTS ON AN XXP+MALEKAMLESH MADAN.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 32; NO 2; PP. 141-142; BIBL. 5 REF.Article

ISODICENTRIC X CHROMOSOME IN A WOMAN WITH CHARACTERISTICS OF GONADAL DYSGENESISLACA Z; IVANOVIC M; DRAMUSIC V et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 237-241; BIBL. 7 REF.Article

Dermatoglyphic findings in patients with fragile X-chromosomeHIRTH, L; SINGH, S; SCHILLING, S et al.Clinical genetics. 1985, Vol 27, Num 2, pp 118-121, issn 0009-9163Article

Inactivation and reactivation of the mammalian X-chromosome ― on the threshold of molecular biologyMARSHALL GRAVES, J. A.Development in mammals. 1983, Vol 5, pp 251-295, issn 0165-2168Article

Integrated kinetics of X chromosome inactivation in differentiating embryonic stem cellsCHAUMEIL, J; OKAMOTO, I; GUGGIARI, M et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 75-84, issn 1424-8581, 10 p.Article

SU UN CASO DI POLISOMIA X A 49 CROMOSOMI (SINDROME 49XXXXY) = SUR UN CAS DE POLYSOMIE X A 49 CHROMOSOMES (SYNDROME 49XXXXY)GARAU A; CRISPONI GG; FLORIS G et al.1974; MINERVA PEDIATR.; ITAL.; DA. 1974; VOL. 26; NO 25; PP. 1249-1259; ABS. ANGL.; BIBL. 1 P. 1/2Article

HUMAN X CHROMOSOME CARRIES QUANTITATIVE GENES FOR IMMUNOGLOBULIN M = LE CHROMOSOME X HUMAIN PORTE DES GENES QUANTITATIFS POUR L'IMMUNOGLOBULINE M1972; SCIENCE; U.S.A.; DA. 1972; VOL. 176; NO 4302; PP. 311-312; BIBL. 10REF.Serial Issue

CHIMAERAS AND CELL LINEAGE IN DEVELOPMENTLEWIS JH; SUMMERBELL D; WOLPERT L et al.1972; NATURE; G.B.; DA. 1972; VOL. 239; NO 5370; PP. 276-279; BIBL. 14REF.Serial Issue

PRIMARY AMENORRHEA WITH A NEW MOSAIC 46, XXQI/47, XXQI XP-. CONSIDERATION ON THE X ISOCHROMOSOME FORMATION AND X CHROMOSOME INACTIVATION.HALBRECHT I; SHABTAI F; KUPFERSTAIN C et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 1; PP. 63-69; ABS. ITAL. FR. ALLEM.; BIBL. 20 REF.Article

MICROFLUOROMETRIC ANALYSIS OF DNA REPLICATION IN HUMAN X CHROMOSOMES = ANALYSE MICROFLUOROMETRIQUE DE LA REPLICATION DE L'ADN DANS DES CHROMOSOMES X HUMAINSLATT SA.1974; EXPER. CELL. RES.; U.S.A.; DA. 1974; VOL. 86; NO 2; PP. 412-415; BIBL. 17REF.Article

STRUCTURAL ABERRATIONS OF THE X CHROMOSOME IN MAN.DAVIDENKOVA EF; VERLINSKAJA DK; MASHKOVA MV et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 269-279; BIBL. 19 REF.Article

Skewed X inactivation in X-linked disordersVAN DEN VEYVER, Ignatia B.Seminars in reproductive medicine. 2001, Vol 19, Num 2, pp 183-191Article

What causes the abnormal phenotype in a 49,XXXXY male?SARTO, G. E; OTTO, P. G; KUHN, E. M et al.Human genetics. 1987, Vol 76, Num 1, pp 1-4, issn 0340-6717Article

On telomere replication and fusion in eukaryotes: apropos of a case of 45,X/46,X,ter rea(X;X)(p22.3;p22.3)RIVERA, H; SOLE, M. T; GARCIA-CRUZ, D et al.Cytogenetics and cell genetics. 1984, Vol 38, Num 1, pp 23-28, issn 0301-0171Article

A fragile X suppressor in the normal human blood?SOUDEK, D; EMANUEL, M.Human genetics. 1983, Vol 65, Num 1, pp 88-89, issn 0340-6717Article

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