452 related articles for article (PubMed ID: 9543547)
1. 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]
2. [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]
3. 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]
4. A clinical and cytogenetic study of Turner syndrome.
Suri M; Kabra M; Jain U; Sanders V; Saxena R; Shukla A; Singh GV; Verma IC
Indian Pediatr; 1995 Apr; 32(4):433-42. PubMed ID: 8635807
[TBL] [Abstract][Full Text] [Related]
5. G-11 staining in Turner's syndrome with mos 45,X/46,X,r(?).
de Almeida JC; Llerena JC; Molina Gomes D; Rita Martins R; Jung M; Reis DF; Cunha AG
Ann Genet; 1985; 28(1):37-41. PubMed ID: 2409888
[TBL] [Abstract][Full Text] [Related]
6. Molecular study of 45,X conceptuses: correlation with clinical findings.
Lorda-Sanchez I; Binkert F; Maechler M; Schinzel A
Am J Med Genet; 1992 Feb; 42(4):487-90. PubMed ID: 1351700
[TBL] [Abstract][Full Text] [Related]
7. PCR detection of Y-specific sequences in patients with Ullrich-Turner syndrome: clinical implications and limitations.
Osipova GR; Karmanov ME; Kozlova SI; Evgrafov OV
Am J Med Genet; 1998 Apr; 76(4):283-7. PubMed ID: 9545090
[TBL] [Abstract][Full Text] [Related]
8. Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
Polityko AD; Khurs OM; Kulpanovich AI; Mosse KA; Solntsava AV; Rumyantseva NV; Naumchik IV; Liehr T; Weise A; Mkrtchyan H
Eur J Med Genet; 2009; 52(4):207-10. PubMed ID: 19375526
[TBL] [Abstract][Full Text] [Related]
9. Cytogenetic findings in 125 patients with Turner's syndrome and abnormal karyotypes.
Coco R; Bergada C
J Genet Hum; 1977 Jun; 25(2):95-107. PubMed ID: 915489
[TBL] [Abstract][Full Text] [Related]
10. Sex chromosome mosaicism of X/XY or X/XY/XYY.
Wilson MG; Ebbin AJ; Shinno NW; Towner JW
Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222
[TBL] [Abstract][Full Text] [Related]
11. [Y chromosome structural abnormalities and Turner's syndrome].
Ravel C; Siffroi JP
Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
[TBL] [Abstract][Full Text] [Related]
12. Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome.
Quilter CR; Taylor K; Conway GS; Nathwani N; Delhanty JD
Ann Hum Genet; 1998 Mar; 62(Pt 2):99-106. PubMed ID: 9759471
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.
Kleczkowska A; Dmoch E; Kubien E; Fryns JP; Van den Berghe H
Genet Couns; 1990; 1(3-4):227-33. PubMed ID: 2098046
[TBL] [Abstract][Full Text] [Related]
14. X microchromosome with additional chromosome anomalies found in Ullrich-Turner syndrome.
Wydner KL; Li M; Singer-Granick C; Sciorra LJ; Krueger LJ
Am J Med Genet; 1995 Mar; 56(2):141-6. PubMed ID: 7625435
[TBL] [Abstract][Full Text] [Related]
15. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
Lin CC; Meyne J; Sasi R; Bowen P; Unger T; Tainaka T; Hadro TA; Hoo JJ
Am J Med Genet; 1990 Sep; 37(1):71-8. PubMed ID: 2240047
[TBL] [Abstract][Full Text] [Related]
16. Detection of cryptic Y chromosome mosaicism by coamplification PCR with archived cytogenetic slides of suspected Turner syndrome.
Kim JW; Cho EH; Kim YM; Kim JM; Han JY; Park SY
Exp Mol Med; 2000 Mar; 32(1):38-41. PubMed ID: 10762060
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetic study of primary amenorrhoea.
Roy AK; Banerjee D
J Indian Med Assoc; 1995 Aug; 93(8):291-2. PubMed ID: 8713239
[TBL] [Abstract][Full Text] [Related]
20. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
Canto P; Kofman-Alfaro S; Jiménez AL; Söderlund D; Barrón C; Reyes E; Méndez JP; Zenteno JC
Cancer Genet Cytogenet; 2004 Apr; 150(1):70-2. PubMed ID: 15041227
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
