108 related articles for article (PubMed ID: 3190016)
1. [Study of isochromosomes of the long arms of the X chromosome].
Borrego S; Fernández-Novoa C; San Martín V; Novales A; Hevia A; Galera H
An Esp Pediatr; 1988 Aug; 29(2):117-21. PubMed ID: 3190016
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. 46,X,i(Xq)/47,XX,+13 mosaicism.
Igarashi M; Tsukahara M; Sugio Y; Katayama K; Kajii T
Ann Genet; 1985; 28(4):241-4. PubMed ID: 3879438
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. [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]
9. 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]
10. Variant Turner features in a female with X-isochromosome [46,X, i(Xq)]: is it a distinct clinical entity?
Verma RS; Vedbrat S; Khan F; Dosik H
Ann Genet; 1981; 24(1):57-60. PubMed ID: 6971622
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Turner syndrome: mosaic and isochromosome q in a young African woman].
Mensah-Ado I; Lauhbouet MD; Lokrou A; Ehouman A; Morlier G
Med Trop (Mars); 1994; 54(4):349-51. PubMed ID: 7746129
[TBL] [Abstract][Full Text] [Related]
13. [Isochromosome X with long branches in two patients with Turner's syndrome].
Nikezić M; Jokanović R; Ajdarić B; Garzicić B; Necić S
Srp Arh Celok Lek; 1978 May; 106(5):553-61. PubMed ID: 751241
[No Abstract] [Full Text] [Related]
14. [X isochromosomes: delayed diagnosis of Turner's syndrome].
Cuesta Hernández M; Rueda Valencia ME; Pérez Rodríguez O; López de Lara D
An Pediatr (Barc); 2015 Jan; 82(1):e131-4. PubMed ID: 25475905
[TBL] [Abstract][Full Text] [Related]
15. [Iso-X chromosomes in primary amenorrhoea and Turner's syndrome - presentation by C-banding (author's transl)].
Zernahle K
Zentralbl Gynakol; 1980; 102(3):151-60. PubMed ID: 7211028
[TBL] [Abstract][Full Text] [Related]
16. H-Y antigen in XO/X,iso(X) mosaic Turner syndrome.
Meade KW; Wachtel SS; Davis JR; Lightner ES
Obstet Gynecol; 1981 May; 57(5):594-9. PubMed ID: 7194461
[TBL] [Abstract][Full Text] [Related]
17. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
González-del-Angel A; Blanco B; del Castillo V; Carnevale A
Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
[TBL] [Abstract][Full Text] [Related]
18. [Molecular cytogenetic study of Turner's syndrome with the 45, X/46,X,r(?) karyotype].
Shi Y; Shi H; Ma S
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1994 Jun; 16(3):218-21. PubMed ID: 7805169
[TBL] [Abstract][Full Text] [Related]
19. 46, X, del (X) (p21) in a 14-year-old female with Turner signs, one streak and one normal ovary.
Crisalli M; Cuoco C; Gimelli G; Monteverde R
Ann Genet; 1981; 24(2):114-6. PubMed ID: 6977291
[No Abstract] [Full Text] [Related]
20. Ullrich-Turner syndrome (45,X/46,X,i[Xq]) in a child with a familial inversion of chromosome 3.
Stine SB; Clark CE; Telfer MA; Casey PA; Cowell HR
Am J Med Genet; 1982 May; 12(1):57-62. PubMed ID: 7091197
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
