These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
120 related articles for article (PubMed ID: 939557)
1. Isochromosome X in man: different DNA replication patterns in the long arms. Baranovskaya LI; Egolina NA; Zakharov AF; Tsvetkova TG Hum Genet; 1976 Jul; 33(1):55-60. PubMed ID: 939557 [TBL] [Abstract][Full Text] [Related]
2. Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq). Yanagisawa S; Yokoyama H Clin Genet; 1975 Apr; 7(4):299-303. PubMed ID: 47795 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Dicentric X isochromosomes in man. Howell RT; Roberts SH; Beard RJ J Med Genet; 1976 Dec; 13(6):496-500. PubMed ID: 1018308 [TBL] [Abstract][Full Text] [Related]
5. Non-fluorescent Y chromosome in a male infant with Turner's symptoms and XO/XY mosaicism. Fonatschi C; Flatz SD; Freymann R Clin Genet; 1977 Mar; 11(3):235-40. PubMed ID: 65235 [TBL] [Abstract][Full Text] [Related]
6. X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere. Maraschio P; Scappaticci S; Ferrari E; Fraccaro M Ann Genet; 1977 Sep; 20(3):179-83. PubMed ID: 304701 [TBL] [Abstract][Full Text] [Related]
7. Isochromosome-X in man. II. Ockey CH; Wennström J; De la Chapelle A Hereditas; 1966; 54(3):277-92. PubMed ID: 6001836 [No Abstract] [Full Text] [Related]
8. [Structure-function features of the long-arm iso-X-chromosome of 45, X/46X, i(Xq) patients]. Beniush VA; Baranovskaia LI; Mirzaiants GG Genetika; 1975; 11(12):102-9. PubMed ID: 1225750 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
12. 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]
13. Chromosomes and DNA of Mus: terminal DNA synthetic sequences in three species. Hsu TC; Markvong A Chromosoma; 1975 Aug; 51(4):311-22. PubMed ID: 1175451 [TBL] [Abstract][Full Text] [Related]
14. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes. Daniel A; Lyons N; Casey JH; Gras L Hum Genet; 1980; 54(1):31-9. PubMed ID: 7190126 [TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. Study on the relationship between cytogenetics and phenotypic effect in Turner's syndrome. Hu X; Zhu B; Lin H; Shu D; Tao D; Wang M J Tongji Med Univ; 1996; 16(4):245-8. PubMed ID: 9389092 [TBL] [Abstract][Full Text] [Related]
18. Isochromosome Yq in a woman with atypical Turner's syndrome. Lønberg NC; Erlendsson J; Nielsen J; Saldaña-Garcia P; Philip J Hum Genet; 1977 Aug; 38(1):49-55. PubMed ID: 561748 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Analysis of the origin of Turner's syndrome using polymorphic DNA probes. Loughlin SA; Redha A; McIver J; Boyd E; Carothers A; Connor JM J Med Genet; 1991 Mar; 28(3):156-8. PubMed ID: 2051451 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]