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.
161 related articles for article (PubMed ID: 7590699)
1. Detection of chromosomal abnormalities in the dysmorphic fetus using fluorescence in situ hybridization: evaluation for monosomy X genotype. Slagel DD; Bromley CM; Benda JA Hum Pathol; 1995 Nov; 26(11):1241-4. PubMed ID: 7590699 [TBL] [Abstract][Full Text] [Related]
2. Association of intrauterine growth retardation with monosomy of the terminal segment of the short arm of the X chromosome in patients with Turner's syndrome. Yaegashi N; Uehara S; Ogawa H; Hanew K; Igarashi A; Okamura K; Yajima A Gynecol Obstet Invest; 2000; 50(4):237-41. PubMed ID: 11093045 [TBL] [Abstract][Full Text] [Related]
3. [Detection of mosaicism in women with Turner's syndrome using fluorescence in situ hybridization]. Zemanová Z; Musilová J; Kurková S; Mayerová K; Pacovská K; Michalová K Cas Lek Cesk; 1999 Jun; 138(13):396-400. PubMed ID: 10566209 [TBL] [Abstract][Full Text] [Related]
4. Molecular diagnosis of Turner's syndrome. Gicquel C; Cabrol S; Schneid H; Girard F; Le Bouc Y J Med Genet; 1992 Aug; 29(8):547-51. PubMed ID: 1355559 [TBL] [Abstract][Full Text] [Related]
5. Fetal cystic hygroma and Turner's syndrome. Carr RF; Ochs RH; Ritter DA; Kenny JD; Fridey JL; Ming PM Am J Dis Child; 1986 Jun; 140(6):580-3. PubMed ID: 3706240 [TBL] [Abstract][Full Text] [Related]
6. Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome. Pasquino AM; Passeri F; Pucarelli I; Segni M; Municchi G J Clin Endocrinol Metab; 1997 Jun; 82(6):1810-3. PubMed ID: 9177387 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. 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]
10. [Application of fluorescence in situ hybridization combined with chromosomal karyotyping analysis in children with disorders of sex development due to sex chromosome abnormalities]. Wang G; Wang J; Zhang Z; Li R; Li L; Li D; Zhang W; Zhang Y; Wang M Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):947-953. PubMed ID: 37532493 [TBL] [Abstract][Full Text] [Related]
12. Laparoscopy in endocrine and genetic disorders of the gonads. Minozzi M; Faggiano M; Jori GP; Lombardi G Acta Endocrinol Suppl (Copenh); 1975; 192():1-124. PubMed ID: 123111 [TBL] [Abstract][Full Text] [Related]
14. Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality. MacFaul R; Turner T; Mason MK Arch Dis Child; 1981 Dec; 56(12):962-3. PubMed ID: 6460476 [TBL] [Abstract][Full Text] [Related]
15. A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn female. Palka G; Calabrese G; Stuppia L; Guanciali Franchi P; Morizio E; Peila R; Antonucci A Clin Genet; 1994 Feb; 45(2):93-6. PubMed ID: 8004805 [TBL] [Abstract][Full Text] [Related]
16. Cytogenetic and molecular findings in patients with Turner's syndrome stigmata. Kuznetzova T; Baranov A; Schwed N; Ivaschenko T; Malet P; Giollant M; Savitsky GA; Baranov V J Med Genet; 1995 Dec; 32(12):962-7. PubMed ID: 8825925 [TBL] [Abstract][Full Text] [Related]
17. Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities. Daggag H; Srour W; El-Khateeb M; Ajlouni K Sex Dev; 2013; 7(6):295-302. PubMed ID: 23988405 [TBL] [Abstract][Full Text] [Related]
18. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations]. Ulmer R; Pfeiffer RA; Kollert A; Beinder E Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179 [TBL] [Abstract][Full Text] [Related]