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.
2. [Monosomy X in mosaicism. II. (XO-XY,XO-XY-XXY,SO-XY-?XXY)]. Izakovic V Bratisl Lek Listy; 1970 Feb; 53(2):195-206. PubMed ID: 5432219 [No Abstract] [Full Text] [Related]
3. Sex chromosome mosaicism of X/XY or X/XY/XYY. Wilson MG; Ebbin AJ; Shinno NW; Towner JW Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution. Hustinx TW; Haar BG; Scheres JM; Rutten FJ Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287 [No Abstract] [Full Text] [Related]
6. [Ring chromosomes in mosaicism 46, XY, Cr-46, XY]. Ferrier S; Freund M; Grétillat A Arch Genet (Zur); 1973; 46(1):1-14. PubMed ID: 4731928 [No Abstract] [Full Text] [Related]
7. Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome. Zamboni G; Bernardi F; Danesino C; del Majno UM; Beghini G; Dalla Bernardina B J Med Genet; 1980 Feb; 17(1):59-61. PubMed ID: 7365765 [TBL] [Abstract][Full Text] [Related]
8. 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]
10. Sex chromosome mosaicism not detected at amniocentesis. Roland B; Cox DM; Rudd NL Prenat Diagn; 1990 May; 10(5):333-6. PubMed ID: 2143821 [TBL] [Abstract][Full Text] [Related]
11. [Triploidy in the child. I. Study of phenotype. An observation of triploidy with mosaicism 46, XX/69, XXY]. David M; Chambon A; Laurent C; Plauchu H; Lindner D; Rouchon A; de Peretti E; Genoud J; Jeune M Pediatrie; 1975; 30(3):281-98. PubMed ID: 1237118 [No Abstract] [Full Text] [Related]
12. [45 X-46 XX-47 XXX mosaic with Turner phenotype and normal ovaries. Study of a case and review of the literature]. Canlorbe P; Toublanc JE; Borniche P; de Grouchy J Ann Pediatr (Paris); 1972 Dec; 19(12):861-6. PubMed ID: 4646742 [No Abstract] [Full Text] [Related]
13. A child with multiple congenital malformations and a 46,XX,t(Bq+;Dq-)-45,XX,-B,-D,+der(B),t(Bq+;Dq-) karyotype. Carnevale A; De los Cobos L J Med Genet; 1973 Dec; 10(4):376-9. PubMed ID: 4359604 [TBL] [Abstract][Full Text] [Related]
14. Three cases of sex chromosome mosaicism with a nonfluorescent Y. Madan K; Gooren L; Schoemaker J Hum Genet; 1979 Feb; 46(3):295-304. PubMed ID: 437772 [TBL] [Abstract][Full Text] [Related]
15. Sex chromosome aberrations in childhood. II. 45,X and 45,X-mosaics. Kiss P; Osztovics M; Erényi J; Orley J Acta Paediatr Acad Sci Hung; 1972; 13(1):1-17. PubMed ID: 4652493 [No Abstract] [Full Text] [Related]
16. Increasing role of cytogenetics in pediatric practice. Dayakar S; Rani DS; Babu SJ; Srilatha K; Jayanthi U; Goud KI; Jain D; Raina V Genet Test Mol Biomarkers; 2010 Apr; 14(2):197-204. PubMed ID: 20384456 [TBL] [Abstract][Full Text] [Related]
20. "Mixed" gonadal dysgenesis, a case with male phenotype and 45,X-46,XY mosaicism. Hortling H; De la Chapelle A; Teppo L; Kivioja O Acta Endocrinol (Copenh); 1970 Oct; 65(2):229-43. PubMed ID: 5535982 [No Abstract] [Full Text] [Related] [Next] [New Search]