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.
187 related articles for article (PubMed ID: 7205197)
1. [Telomeric fusion of the short arms of both X chromosomes in a patient presenting an atypical Turner syndrome]. Pescia G; Jotterand-Bellomo M; Nguyen TH; Scholberg-Hermann B J Genet Hum; 1980 Dec; 28(4):131-40. PubMed ID: 7205197 [TBL] [Abstract][Full Text] [Related]
3. An abnormal dicentric X chromosome in a patient with short stature and gonadal dysgenesis. Smith A; Donnelly PE; Elliott G; den Dulk G Ann Genet; 1979; 22(3):143-7. PubMed ID: 316668 [TBL] [Abstract][Full Text] [Related]
4. Center for Barr body condensation. A case of Turner's syndrome with 45,X/46,X,dic(X) (Xqter leads to p22::p22 leads to qter). Sillesen I; Rasmussen K; Osterballe O; Nielsen J Hum Genet; 1976 Aug; 33(3):337-40. PubMed ID: 964996 [TBL] [Abstract][Full Text] [Related]
5. Turner's syndrome with XO/XXp- karyotype: a case report. Koller AB; Rubin A S Afr Med J; 1976 Sep; 50(38):1484-6. PubMed ID: 973169 [TBL] [Abstract][Full Text] [Related]
6. Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome. Binder G; Eggermann T; Enders H; Ranke MB; Dufke A J Pediatr; 2001 Feb; 138(2):285-7. PubMed ID: 11174634 [TBL] [Abstract][Full Text] [Related]
7. A case of 45,X/46,X,dic(X)(qter----p22::p22----qter) with Turner's phenotype in a Japanese girl. Takenaka M; Teramoto H; Ueda K; Fujiwara A; Ohama K; Nishi Y Hiroshima J Med Sci; 1988 Jun; 37(2):51-5. PubMed ID: 3170251 [No Abstract] [Full Text] [Related]
8. [A report of 2 cases of Turner's syndrome with a ring X chromosome]. Migliori MV; Bartolotta E; Maurizi M; Bonazzi P; Cardinale G; Manunza V Minerva Pediatr; 1991 Sep; 43(9):605-9. PubMed ID: 1758399 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation. Bjerglund Nielsen L; Nielsen IM Ann Genet; 1984; 27(3):173-7. PubMed ID: 6334482 [TBL] [Abstract][Full Text] [Related]
11. Cri du chat and Turner syndrome features in a newborn girl with an unbalanced 45,X,psu dic(5;X)(p15.2;p22.1) karyotype: FISH and replication banding studies. Reddy KS; Smith DL; Ball CS Ann Genet; 1999; 42(2):105-8. PubMed ID: 10434125 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. [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]
14. Evaluation of sex chromosome aneuploidies in women with Turner's syndrome by G-banding and FISH. A serial case study. Cortés-Gutiérrez EI; Cerda-Flores RM; Silva-Cudish JB; Dávila-Rodríguez MI; Hernández-Herrera R; Leal-Garza CH J Reprod Med; 2003 Oct; 48(10):804-8. PubMed ID: 14628733 [TBL] [Abstract][Full Text] [Related]
15. A nonmosaic 45,X karyotype in a mother with Turner's syndrome and in her daughter. Cools M; Rooman RP; Wauters J; Jacqemyn Y; Du Caju MV Fertil Steril; 2004 Oct; 82(4):923-5. PubMed ID: 15482770 [TBL] [Abstract][Full Text] [Related]
16. Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome. Burégio-Frota P; Valença L; Leal GF; Duarte AR; Bispo-Brito AV; Soares-Ventura EM; Marques-Salles TJ; Nogueira MT; Muniz MT; Silva ML; Hunstig F; Liehr T; Santos N Genet Mol Res; 2010 Apr; 9(2):780-4. PubMed ID: 20449811 [TBL] [Abstract][Full Text] [Related]
18. Telomeric fusion and chromosome instability in multiple tissues of a patient with mosaic Ullrich-Turner syndrome. Sawyer JR; Swanson CM; Lukacs JL; Hassed SJ; Curtis MA; North PE; Kozlowski KJ; Pihoker C Am J Med Genet; 1997 Apr; 69(4):383-7. PubMed ID: 9098487 [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. [A second case of (de novo) paracentric inversion of the short arm of the X chromosome]. Dahoun S Ann Genet; 1990; 33(1):52-5. PubMed ID: 2195983 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]