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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- Byrd J R, Askew D E, McDonough P G: Cytogenetic findings in fifty-five couples with recurrent fetal wastage. Fert. Ster. 28:246-250, 1977. [PubMed: 557002]Case 2 E. B. in this report.46,XY,t(1;9)(p3;p2).Aberration: Simple translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)No band
- Diedrich U, Hansmann I, Janke D, Opitz O, Probeck H D: Chromosome anomalies in 136 couples with a history of recurrent abortions. Hum. Genet. 65:48-52, 1983. [PubMed: 6642507]46,XX,rcp(1;16)(p3;p1).Aberration: Reciprocal translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)No band
- Kjessler B, Gustavson K H, Wigertz A: Apparently non-deleted ring-1 chromosome and extreme growth failure in a mentally retarded girl. Clin. Genet. 14:8-15, 1978. [PubMed: 679524]46,XX,r(1)(p3q4).Aberration: Ring chromosomeNo band
- Nuzzo F, Giorgi R, Zuffardi O, Dambrosio F: "Translocation t(1p+;2q-) associated with recurrent abortion." Ann. Genet. 16:211-214, 1973. [PubMed: 4543211]46,XX,t(1;2)(p3;q1).Aberration: Simple translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)No band
- Stenchever M A, Parks K J, Daines T L, Allen M A, Stenchever M R: Cytogenetics of habitual abortion and other reproductive wastage. Am. J. Obst. Gynecol. 127:143-150, 1977. [PubMed: 556663]46,XX/46,XX,t(1p+;2q-) (50% of the blood cells).&"46,XX,t(1p+;17q-)."&Karyotyping data are not entirely clear in this report.Aberration: Simple translocationIndex Terms: Fetal wastage (Habitual recurrent, spontaneous abortion)No band
- Tartaglia A P, Propp S, Amarose A P, Propp R P, Hall C A: Chromosome abnormality and hypocalcemia in congenital erythroid hypoplasia (Blackfan-Diamond syndrome). Am. J. Med. 41:990-999, 1966. [PubMed: 5954459]A gap was reported in this region.MIM#: 205900Index Terms: Blackfan-Diamond syndrome,HypocalcemiaNo band
- 01p300 - Chromosomal Variation in Man01p300 - Chromosomal Variation in Man
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