120 related articles for article (PubMed ID: 1544315)
1. 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]
2. A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes.
Gilgenkrantz S; Briquel ME; Mandel JL; Oberle I
Hum Genet; 1986 Feb; 72(2):157-9. PubMed ID: 3455922
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.
Scott SA; Cohen N; Brandt T; Warburton PE; Edelmann L
Hum Mol Genet; 2010 Sep; 19(17):3383-93. PubMed ID: 20570968
[TBL] [Abstract][Full Text] [Related]
5. Inversion of intron 22 of the factor VIII gene in a girl with severe hemophilia A and Turner's syndrome.
Chuansumrit A; Sasanakul W; Goodeve A; Treratvirapong T; Parinayok R; Pintadit P; Hathirat P
Thromb Haemost; 1999 Oct; 82(4):1379. PubMed ID: 10544944
[No Abstract] [Full Text] [Related]
6. Severe hemophilia in a girl infant with mosaic Turner syndrome and persistent hyperplastic primary vitreous.
Shahriari M; Bazrafshan A; Moghadam M; Karimi M
Blood Coagul Fibrinolysis; 2016 Apr; 27(3):352-3. PubMed ID: 26484646
[TBL] [Abstract][Full Text] [Related]
7. Replication patterns of three isodicentric X chromosomes and an X isochromosome in human lymphocytes.
Dewald G; Spurbeck JL; Gordon H
Am J Med Genet; 1978; 1(4):445-60. PubMed ID: 665728
[TBL] [Abstract][Full Text] [Related]
8. De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.
Chelly J; Marlhens F; Le Marec B; Jeanpierre M; Lambert M; Hamard G; Dutrillaux B; Kaplan JC
Hum Genet; 1986 Oct; 74(2):193-6. PubMed ID: 2876949
[TBL] [Abstract][Full Text] [Related]
9. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Factor VIII gene mutations and RFLP analysis in hemophilia A.
Krepelová A; Brdicka R; Vorlová Z
Stem Cells; 1993 May; 11 Suppl 1():72-6. PubMed ID: 8100465
[TBL] [Abstract][Full Text] [Related]
12. A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype.
Dundar M; Lowther G; Acar H; Kurtoglu S; Demiryilmaz F; Kucukaydin M
Ann Genet; 2001; 44(1):5-8. PubMed ID: 11334610
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Hemophilia A and factor V deficiency in a girl with Turner syndrome: a case report.
Al Khudari R; Batesh D; Habash R; Hamdn O
J Med Case Rep; 2023 Nov; 17(1):480. PubMed ID: 37978530
[TBL] [Abstract][Full Text] [Related]
15. Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere-fra(X)-DXS15-DXS52-F8C-telomere.
Mulligan LM; Grover HJ; Blanchette VS; Giles AR; Lillicrap DP; Phillips A; Holden JJ; White BN
Am J Med Genet; 1987 Mar; 26(3):751-60. PubMed ID: 3105317
[TBL] [Abstract][Full Text] [Related]
16. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
17. Severe haemophilia A in a female: a compound heterozygote with nonrandom X-inactivation.
Seeler RA; Vnencak-Jones CL; Bassett LM; Gilbert JB; Michaelis RC
Haemophilia; 1999 Nov; 5(6):445-9. PubMed ID: 10583534
[TBL] [Abstract][Full Text] [Related]
18. Haemophilia A: the consequences of de novo mutations. Two case reports.
Zarrilli F; Coppola A; Schiavulli M; Cimino E; Elce A; Rescigno G; Castaldo G; Amato F
Blood Transfus; 2018 Jul; 16(4):392-393. PubMed ID: 28488976
[No Abstract] [Full Text] [Related]
19. Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosome.
Tassanakijpanich N; Wright R; Tassone F; Shankar SP; Hagerman R
BMJ Case Rep; 2022 Jul; 15(7):. PubMed ID: 35882436
[TBL] [Abstract][Full Text] [Related]
20. The impact of concurrent X chromosome anomalies on diagnosis and bleeding phenotype in children with hemophilia: A single-institution case series.
Soffer E; Coleman K; Batsuli G
Pediatr Blood Cancer; 2023 Jul; 70(7):e30400. PubMed ID: 37132158
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]