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Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.
Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].
Show details- Petrosky D L, Borgaonkar D S: Segregation analysis in reciprocal translocation carriers. AJMG 19:137-159, 1984. [PubMed: 6496566]No band
- Sarto G E: Cytogenetics of fifty patients with primary amenorrhea. Am. J. Obst. Gynecol. 119:14-23, 1974. [PubMed: 4820908]46,XX,t(10q+;12q-).Aberration: Simple translocationNo band
- Schanzlin D J, Goldberg D B, Brown S I: Hallerman-Streiff syndrome associated with sclerocornea, aniridia, and a chromosome abnormality. Am. J. Opthal. 90:411-415, 1980. [PubMed: 6999913]46,XY,10q+.&Parental karyotypes were normal. A second cousin with the Hallerman-Streiff syndrome had normal karyotype.MIM#: 234100Index Terms: Aniridia,SclerocorneaNo band
- Storto P D, Diehn T N, O''Malley D P, Bullard B A, Netzloff M L, Van Dyke D L, Feldman G L, Precht K S, Ledbetter D H, Lese C M.: Satellited chromosome 10 detected prenatally in a fetus and confirmed as mosaic in a patient. Prenat. Diag. 19:1088-1089, 1999. [PubMed: 10589072]Mother was a gravida 1 patient referred because of advanced maternal age.46,XX,der(10qs)pat.The pregnancy resulted in a normal outcome.Aberration: Marker chromosomeIndex Terms: Satellited 10q
- Verma R S, Peakman D C, Robinson A, Lubs H A: Comparison of G-, Q-, and R-banding in 28 cases of chromosomal abnormalities. Cytogenet. Cell Genet. 16:479-486, 1976. [PubMed: 975933]Case No. 744 in this report.46,XX,10q+.No band
- 10q000 - Chromosomal Variation in Man10q000 - Chromosomal Variation in Man
- Chain M, Eukaryotic translation initiation factor 3 subunit MChain M, Eukaryotic translation initiation factor 3 subunit Mgi|699027402|pdb|3J8C|MProtein
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