Gonadoblastoma in a patient with an isodicentric X chromosomeKATAYAMA, K. P; ROESLER, M. R; DUNGAR, C. F et al.Clinical genetics. 1983, Vol 24, Num 5, pp 355-358, issn 0009-9163Article

Replication and inactivation of an isodicentric X: presence of an inactive centromere influences the replication patternsFRYNS, J. P; PETIT, P; KLECZKOWSKA, A et al.Clinical genetics. 1983, Vol 24, Num 3, pp 180-183, issn 0009-9163Article

Interstitial deletion in the critical region of the long arm of the X chromosome in a mentally retarded boy and his normal motherTABOR, A; ANDERSEN, O; LUNDSTEEN, C et al.Human genetics. 1983, Vol 64, Num 2, pp 196-199, issn 0340-6717Article

X chromosome replication patterns in a case of X; 9 balanced translocationFILIPPI, G; PECILE, V; ARCHIDIACONO, N et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 467-468, issn 0022-2593Article

Inversion péricentrique familiale du chromosome X [inv(X)(p11q28)] = Familial pericentric inversion of X chromosome inv(X)(p11q28)BAUMANN, W; ZABEL, B; HOLL, M et al.Annales de génétique (Paris). 1984, Vol 27, Num 2, pp 106-108, issn 0003-3995Article

The phenotypic effects of SMALL, distal Xq deletionsTRUNCA, C; THERMAN, E; ROSENWAKS, Z et al.Human genetics. 1984, Vol 68, Num 1, pp 87-89, issn 0340-6717Article

De novo paracentric inversion in an X chromosomeHERR, H. M; HORTON, S. J; SCOTT, C. I. JR et al.Journal of medical genetics. 1985, Vol 22, Num 2, pp 140-142, issn 0022-2593Article

X long-arm deletions. A review of non-mosaic cases studied with banding techniquesSKIBSTED, L; WESTH, H; NIEBUHR, E et al.Human genetics. 1984, Vol 67, Num 1, pp 1-5, issn 0340-6717Article

Two new X-autosome translocations in the mouseSEARLE, A. G; BEECHEY, C. V; EVANS, E. P et al.Cytogenetics and cell genetics. 1983, Vol 35, Num 4, pp 279-292, issn 0301-0171Article

Overall DNA methylation and chromatin structure of normal and abnormal X chromosomesBERNARDINO-SGHERRI, J; FLAGIELLO, D; DUTRILLAUX, B et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 85-91, issn 1424-8581, 7 p.Article

Genetics of inbred Drosophila melanogaster. XII: Effects of an X-chromosome inversion on primary and secondary non-disjunctionLUNING, K. G; LAKE, S; LINDE, M et al.Hereditas (Landskrona). 1984, Vol 100, Num 2, pp 247-257, issn 0018-0661Article

X-Chromosome hyperploidy in couples with multiple spontaneous abortionsHOLZGREVE, W; SCHONBERG, S. A; DOUGLAS, R. G et al.Obstetrics and gynecology (New York. 1953). 1984, Vol 63, Num 2, pp 237-240, issn 0029-7844Article

Etude cytogénétique de 14 cas d'aménorrhéeZHOU HUANGENG; KANG XUEZHEN; ZHANG QINGQING et al.Yíchuán xuébào. 1984, Vol 11, Num 6, pp 494-499, issn 0379-4172Article

Replication patterns of human X isochromosomes by high-resolution bandingARTIFONI, L; BACCICHETTI, C; PIOVAN, E et al.Cytogenetics and cell genetics. 1983, Vol 36, Num 4, pp 649-651, issn 0301-0171Article

X LONG ARM DELETION WITH OLIGOMENORRHOEAMIJIN K; STOLEVIC E; ADZIC S et al.1982; JOURNAL OF MEDICAL GENETICS; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 4; PP. 305-306; BIBL. 13 REF.Article

NOTES ON CLINICAL FEATURES OF A 46, XXP-PATIENTISHITOBI K; NAKADA N; WATANABE A et al.1982; PROCEEDINGS OF THE JAPAN ACADEMY. SERIES B: PHYSICAL AND BIOLOGICAL SCIENCES; ISSN 0386-2208; JPN; DA. 1982; VOL. 63; NO 2; PP. 25-28; BIBL. 10 REF.Article

STRUCTURAL ABNORMALITIES OF THE X-CHROMOSOME IN A HEIFERGENEST P; GUAY P.1979; REV. CANAD. MED. COMP.; CAN; DA. 1979; VOL. 43; NO 1; PP. 110-111; ABS. FRE; BIBL. 3 REF.Article

CLINICAL CONSEQUENCES OF XP-EGOZCUE J.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 1; PP. 141-142; BIBL. 15 REF.Article

MARKER X SYNDROMEHOWARD PEEBLES PN.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 2; PP. 407-408; BIBL. 6 REF.Article

CYTOGENETIC INVESTIGATION OF SIX PATIENTS WITH X ISOCHROMOSOMES, I(XQ), AND OF TWO SUBJECTS WITH ISODICENTRIC X CHROMOSOMES, IDIC(XQ)GAAL M; LASZLO J; BOESZE P et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 362-365; BIBL. 22 REF.Article

HETEROMORPHIC X CHROMOSOMES IN 46, XX MALES.DE LA CHAPELLE A; SIMOLA K; SIMOLA P et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 2; PP. 157-167; BIBL. 10 REF.Article

ISODICENTRIC (X)(Q13): A NEW CHARACTERISTIC CHROMOSOMAL ANOMALY IN MYELOPROLIFERATIVE SYNDROME. = CHROMOSOME ISODICENTRIQUE (X)(Q13): UNE NOUVELLE ANOMALIE CHROMOSOMIQUE CARACTERISTIQUE DANS LE SYNDROME MYELOPROLIFERATIF.PETIT P; FRYNS JP; MASURE R et al.1982; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1982; VOL. 7; NO 4; PP. 339-341; ABS. ENG; BIBL. 3 REF.; FIGArticle

STRUCTURAL ANOMALIES OF THE X CHROMOSOME: PERSONAL OBSERVATION AND REVIEW OF NON-MOSAIC CASESWYSS D; DELOZIER CD; DANIELL J et al.1982; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1982; VOL. 21; NO 2; PP. 145-159; BIBL. 5 P.Article

VARIANT TURNER FEATURES IN A FEMALE WITH X-ISOCHROMOSOME (46, X, I (XQ)): IS IT A DISTINC CLINICAL ENTITY.VERMA RS; VEDBRAT S; KHAN F et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 57-60; ABS. FRE; BIBL. 22 REF.Article

ANALYSIS OF DNA REPLICATION PATTERNS OF HUMAN FIBROBLAST CHROMOSOMES. THE REPLICATION MAP.KONDRA PM; RAY M.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 2; PP. 139-149; BIBL. 2 P.Article