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Journal Abstract Search
77 related items for PubMed ID: 14564053
1. A low-level X chromosome mosaicism in mares, detected by chromosome painting. Wieczorek M, Switoński M, Yang F. J Appl Genet; 2001; 42(2):205-9. PubMed ID: 14564053 [Abstract] [Full Text] [Related]
2. Detection of equine X chromosome mosaicism in a mare using an equine X whole chromosome painting probe (WCPP)--a case report. Bugno M, Słota E, Pieńkowska-Schelling A, Schelling C. Acta Vet Hung; 2007 Jun; 55(2):207-12. PubMed ID: 17555285 [Abstract] [Full Text] [Related]
3. Identification of chromosome abnormalities in the horse using a panel of chromosome-specific painting probes generated by microdissection. Bugno M, Słota E, Pieńkowska-Schelling A, Schelling C. Acta Vet Hung; 2009 Sep; 57(3):369-81. PubMed ID: 19635709 [Abstract] [Full Text] [Related]
4. Chromosome abnormalities as a cause of infertility in mares. Chandley AC, Fletcher J, Rossdale PD, Peace CK, Ricketts SW, McEnery RJ, Thorne JP, Short RV, Allen WR. J Reprod Fertil Suppl; 1975 Oct; (23):377-83. PubMed ID: 1060811 [Abstract] [Full Text] [Related]
5. [Analysis of X chromosome mosaicism in patients with premature ovarian failure by fluorescent in-situ hybridization]. Diao FY, Xu M, Liu JY. Zhonghua Fu Chan Ke Za Zhi; 2003 Jan; 38(1):20-3. PubMed ID: 12757653 [Abstract] [Full Text] [Related]
7. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases]. Zhao L, Li H, Xue YQ, Pan JL, Wu YF, Lu M. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):611-4. PubMed ID: 15583994 [Abstract] [Full Text] [Related]
8. [Screening for Y chromosome sequences in patients with Turner syndrome]. Ferrão L, Lopes ML, Limbert C, Marques B, Boieiro F, Silva M, Marques R, Lavinha J, Mota A, Gonçalves J. Acta Med Port; 2002 Dec; 15(2):89-100. PubMed ID: 15524154 [Abstract] [Full Text] [Related]
11. Cytogenetic studies in amenorrhea. Rajangam S, Nanjappa L. Saudi Med J; 2007 Feb; 28(2):187-92. PubMed ID: 17268694 [Abstract] [Full Text] [Related]
12. 47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development. Brambila-Tapia AJ, Rivera H, García-Castillo H, Domínguez-Quezada MG, Dávalos-Rodríguez IP. Fertil Steril; 2009 Nov; 92(5):1747.e5-7. PubMed ID: 19732877 [Abstract] [Full Text] [Related]
13. Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success. Santos M, Mrasek K, Rigola MA, Starke H, Liehr T, Fuster C. Fertil Steril; 2007 Oct; 88(4):969.e11-7. PubMed ID: 17451694 [Abstract] [Full Text] [Related]
14. Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytes. Röpke A, Pelz AF, Volleth M, Schlösser HW, Morlot S, Wieacker PF. Am J Obstet Gynecol; 2004 Apr; 190(4):1059-62. PubMed ID: 15118641 [Abstract] [Full Text] [Related]
15. Two cases of infertile bitches with 78,XX/77,X mosaic karyotype: a need for cytogenetic evaluation of dogs with reproductive disorders. Switonski M, Szczerbal I, Grewling J, Antosik P, Nizanski W, Yang F. J Hered; 2003 Apr; 94(1):65-8. PubMed ID: 12692164 [Abstract] [Full Text] [Related]
16. Application of droplet digital PCR in diagnosing of X monosomy in mares. Szczerbal I, Nowacka-Woszuk J, Kopp-Kuhlman C, Mackowski M, Switonski M. Equine Vet J; 2020 Jul; 52(4):627-631. PubMed ID: 31793061 [Abstract] [Full Text] [Related]
17. Fertility and 63,X Mosaicism in a Haflinger Sibship. Neuhauser S, Handler J, Schelling C, Pieńkowska-Schelling A. J Equine Vet Sci; 2019 Jul; 78():127-133. PubMed ID: 31203976 [Abstract] [Full Text] [Related]
18. Chromosomal mosaicism mitigates stigmata and cardiovascular risk factors in Turner syndrome. El-Mansoury M, Barrenäs ML, Bryman I, Hanson C, Larsson C, Wilhelmsen L, Landin-Wilhelmsen K. Clin Endocrinol (Oxf); 2007 May; 66(5):744-51. PubMed ID: 17381484 [Abstract] [Full Text] [Related]
19. Further cases of equine sex chromosome abnormalities. Stewart-Scott IA, Pearce PD, Burkin DJ. N Z Vet J; 1990 Jun; 38(2):54-6. PubMed ID: 16031576 [Abstract] [Full Text] [Related]
20. Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection. Weimer J, Shivakumar S, Danda S, Thomas N, Ralui LP, Jonat W, Arnold N. Fertil Steril; 2007 Dec; 88(6):1677.e9-13. PubMed ID: 17482166 [Abstract] [Full Text] [Related] Page: [Next] [New Search]