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4. [Turner's syndrome with mosaic karyotype and renovascular hypertension]. Jelić S; Marisavljević D Srp Arh Celok Lek; 1997; 125(1-2):48-50. PubMed ID: 17974355 [TBL] [Abstract][Full Text] [Related]
5. Pulmonary hypoplasia with an unusual prenatal history. Takahashi R; Kakizawa H; Itow T; Yamada M; Nakae S; Shintaku Y; Nagata M; Nakayama M Pediatr Pulmonol; 2002 Sep; 34(3):218-21. PubMed ID: 12203851 [TBL] [Abstract][Full Text] [Related]
6. [45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome]. Gil R; Galán F; López-Ginés C; Gregori-Romero M; Millet A; Pellín A; Llombart-Bosch A Rev Clin Esp; 1991 Jun; 189(1):23-5. PubMed ID: 1924922 [TBL] [Abstract][Full Text] [Related]
7. [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]
8. Altered fetal growth and development in a patient with Turner's syndrome. Platt LD; Korula SR; DeVore GR; Mishell DR Am J Perinatol; 1986 Jul; 3(3):175-7. PubMed ID: 3718636 [TBL] [Abstract][Full Text] [Related]
9. [Cystic adenomatoid malformation of the lung, bilateral renal agenesis and left heart hypoplasia. An unusual association in Potter's syndrome]. Carles D; Dallay D; Serville F; Maugey-Laulom B; Alberti EM; Tissot H; Weichhold W; Wursten-Guitton F Ann Pathol; 1992; 12(6):367-70. PubMed ID: 1294159 [TBL] [Abstract][Full Text] [Related]
10. Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation. Webb AL; Sturgiss S; Warwicker P; Robson SC; Goodship JA; Wolstenholme J Prenat Diagn; 1996 Oct; 16(10):958-62. PubMed ID: 8938070 [TBL] [Abstract][Full Text] [Related]
12. [Turner's syndrome--case report of a female patient with chromosome mosaicism]. Roglić A; Kastelan D; Kozić-Rukavina B; Korsić M Lijec Vjesn; 1998; 120(7-8):210-2. PubMed ID: 9919878 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. [Turner's syndrome in mother and daughter]. Waelkens JJ Ned Tijdschr Geneeskd; 2004 Jun; 148(24):1208-10. PubMed ID: 15224434 [TBL] [Abstract][Full Text] [Related]
15. Ring chromosome 4 mosaicism and Potter sequence. Fryns JP; Kleczkowska A; Jaeken J; Van den Berghe H Ann Genet; 1988; 31(2):120-2. PubMed ID: 3261147 [TBL] [Abstract][Full Text] [Related]
17. Trisomy 9 mosaicism: another etiology for the manifestations of Goldenhar syndrome. Wilson GN; Barr M J Craniofac Genet Dev Biol; 1983; 3(4):313-6. PubMed ID: 6662905 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of mosaicism identified in amniotic fluid cell cultures. Sahin FI; Yilmaz Z; Uckuyu A; Ozalp O; Tarim E; Deren O; Yanik F Genet Couns; 2006; 17(3):341-8. PubMed ID: 17100203 [TBL] [Abstract][Full Text] [Related]
19. HLHS with severe aortic insufficiency in a patient with 45,X/46,XY mosaicism. Mumtaz MA; Mee RB; Qureshi A; Patel CR; Younoszai AK Ann Thorac Surg; 2004 Oct; 78(4):1475-6. PubMed ID: 15464527 [TBL] [Abstract][Full Text] [Related]
20. Analysis of the SRY gene in a girl with 45,X/46,XY genotype. Akbas E; Soylemez F; Hallioglu O; Polat S; Turkoz G Genet Couns; 2009; 20(3):249-54. PubMed ID: 19852431 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]