114 related articles for article (PubMed ID: 2901328)
1. Molecular studies of the parental origin and nature of human X isochromosomes.
Harbison M; Hassold T; Kobryn C; Jacobs PA
Cytogenet Cell Genet; 1988; 47(4):217-22. PubMed ID: 2901328
[TBL] [Abstract][Full Text] [Related]
2. A molecular study of X isochromosomes: parental origin, centromeric structure, and mechanisms of formation.
Lorda-Sanchez I; Binkert F; Maechler M; Schinzel A
Am J Hum Genet; 1991 Nov; 49(5):1034-40. PubMed ID: 1681727
[TBL] [Abstract][Full Text] [Related]
3. Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.
Callen DF; Mulley JC; Baker EG; Sutherland GR
Hum Genet; 1987 Nov; 77(3):236-40. PubMed ID: 3479386
[TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of isochromosomes of Xq.
James RS; Dalton P; Gustashaw K; Wolff DJ; Willard HF; Mitchell C; Jacobs PA
Ann Hum Genet; 1997 Nov; 61(Pt 6):485-90. PubMed ID: 9543548
[TBL] [Abstract][Full Text] [Related]
5. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.
Wolff DJ; Miller AP; Van Dyke DL; Schwartz S; Willard HF
Am J Hum Genet; 1996 Jan; 58(1):154-60. PubMed ID: 8554051
[TBL] [Abstract][Full Text] [Related]
6. Cytogenetic investigation of six patients with X isochromosomes, i(Xq), and of two subjects with isodicentric X chromosomes, idic (Xq).
Gaál M; László J; Bösze P
Hum Genet; 1981; 58(4):362-5. PubMed ID: 7327558
[TBL] [Abstract][Full Text] [Related]
7. Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52.
Panarello C; Acquila M; Caprino D; Gimelli G; Pecorara M; Mori PG
Cytogenet Cell Genet; 1992; 59(4):241-2. PubMed ID: 1544315
[TBL] [Abstract][Full Text] [Related]
8. [RFLPs study of parental origin and mechanism of 3 cases with X chromosome structural abnormality].
Dai H; Deng H; He X; Li L; Xia J
Yi Chuan Xue Bao; 1992; 19(4):298-303. PubMed ID: 1361346
[TBL] [Abstract][Full Text] [Related]
9. Isodicentric X chromosome and mosaicism: report on two cases of 45,X/46,X,idic(Xq)/47,X,idic(Xq),idic(Xq) and review of the literature.
Melaragno MI; Fakih LM; Cernach MC; Maccagnan P
Am J Med Genet; 1993 Sep; 47(3):357-9. PubMed ID: 8135281
[TBL] [Abstract][Full Text] [Related]
10. [Rare chromosomal aberrations in the Shereshevskiĭ-Turner syndrome].
Shandlorenko SK; Maksimova SP; Verlinskaia DK
Tsitologiia; 1986 Jul; 28(7):748-50. PubMed ID: 3765110
[TBL] [Abstract][Full Text] [Related]
11. Microsatellite analysis in Turner syndrome: parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes.
Monroy N; López M; Cervantes A; García-Cruz D; Zafra G; Canún S; Zenteno JC; Kofman-Alfaro S
Am J Med Genet; 2002 Jan; 107(3):181-9. PubMed ID: 11807897
[TBL] [Abstract][Full Text] [Related]
12. A cytogenetic and molecular study of a series of 45,X fetuses and their parents.
Cockwell A; MacKenzie M; Youings S; Jacobs P
J Med Genet; 1991 Mar; 28(3):151-5. PubMed ID: 1675683
[TBL] [Abstract][Full Text] [Related]
13. Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype.
Uematsu A; Yorifuji T; Muroi J; Kawai M; Mamada M; Kaji M; Yamanaka C; Momoi T; Nakahata T
Am J Med Genet; 2002 Aug; 111(2):134-9. PubMed ID: 12210339
[TBL] [Abstract][Full Text] [Related]
14. The parental origin of the missing or additional chromosome in 45,X and 47,XXX females.
Hassold T; Arnovitz K; Jacobs PA; May K; Robinson D
Birth Defects Orig Artic Ser; 1990; 26(4):297-304. PubMed ID: 1982521
[TBL] [Abstract][Full Text] [Related]
15. Structural aberrations of the X chromosome in man.
Davidenkova EF; Verlinskaja DK; Mashkova MV
Hum Genet; 1978 Apr; 41(3):269-79. PubMed ID: 649155
[TBL] [Abstract][Full Text] [Related]
16. Diagnostic reliability of the cytogenetic centromere heteromorphism in the human X chromosome.
Friedrich U; Larsen TB; Nielsen J
Clin Genet; 1991 Dec; 40(6):465-6. PubMed ID: 1685701
[TBL] [Abstract][Full Text] [Related]
17. Parental origin and mechanism of formation of X chromosome structural abnormalities: four cases determined with RFLPs.
Deng HX; Xia JH; Ishikawa M; Niikawa N
Jinrui Idengaku Zasshi; 1990 Sep; 35(3):245-51. PubMed ID: 1979996
[TBL] [Abstract][Full Text] [Related]
18. Turner syndrome: a cytogenetic and molecular study.
Jacobs P; Dalton P; James R; Mosse K; Power M; Robinson D; Skuse D
Ann Hum Genet; 1997 Nov; 61(Pt 6):471-83. PubMed ID: 9543547
[TBL] [Abstract][Full Text] [Related]
19. Endocrine, cytogenetic and psychometric features of patients with X-isochromosome 46, X, i(Xq) Turner's syndrome: a preliminary study in nine patients.
Zinman B; Kabiawu SI; Moross T; Berg J; Lupmanis A; Markovic V; Gardner HA
Clin Invest Med; 1984; 7(3):135-41. PubMed ID: 6518681
[TBL] [Abstract][Full Text] [Related]
20. Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination.
Lebo RV; Milunsky J; Higgins AW; Loose B; Huang XL; Wyandt HE
Am J Med Genet; 1999 Aug; 85(5):429-37. PubMed ID: 10405438
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]