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Publikováno v:
Journal of Clinical Laboratory Analysis; 1993, Vol. 7 Issue 5, p283-292, 10p
Autor:
Ming–Liang Lee, Demetra V. Rose, Barathur R. Rajendra, Leonard J. Sciorra, Michael J. Nissenblatt, Gary Gartenberg
Publikováno v:
The American Journal of the Medical Sciences. 291:276-279
Essential thrombocytosis is a myeloproliferative disease not known to have consistent cytogenetic abnormalities. A 46-year-old black woman with essential thrombocytosis and a Philadelphia chromosome is reported. Iron deficiency and tuberculosis were
Autor:
Gary Gartenberg, Barathur R. Rajendra, Ming-liang Lee, Leonard J. Sciorra, Michael J. Nissenblatt, Demetra V. Rose
Publikováno v:
Human Genetics. 56:287-291
The Philadelphia chromosome, assessed with banding techniques, was detected in 98.3% of bone marrow cells of a 46-year-old black female presenting with essential thrombocytosis. The patient has been followed for the past two years with no signs of ch
Publikováno v:
American Journal of Medical Genetics. 10:119-131
A 29-year-old infertile man with mild eunuchoid body proportions and unilateral gynecomastia with a low sperm count had normal chromosomes in lymphocytes and skin fibroblasts. Serum testosterone, urinary ketosteroid, and follicle-stimulating hormone
Autor:
Linda Ekblom, Ming-liang Lee, Barathur R. Rajendra, Emilie Cummings, Leonard J. Sciorra, John M. Opitz
Publikováno v:
American Journal of Medical Genetics. 10:147-149
Prenatal chromosome analysis of amniotic cells showed a male fetus to carry an unusual marker D chromosome containing extra genetic material on the short arm, which could be interpreted as a possible t(D;G) or t(D;Fq) unbalanced translocation using n
Publikováno v:
Human Genetics; September 1980, Vol. 55 Issue: 3 p363-366, 4p
Publikováno v:
Human genetics. 59(4)
A rapid culture-harvest technique for amniotic fluid is presented using the poly-L-lysine technique (Rajendra et al. 1980). The procedure is simple, reproducible, and involves harvesting primary cultures five to eight days after culture. This techniq
Publikováno v:
American journal of medical genetics. 25(2)
A premature infant with unilateral aniridia and congenital ectropion uveae, contralateral Rieger anomaly, bilateral congenital glaucoma, and hydrocephalus was found to have ring chromosome 6. The findings are consistent with multiple manifestations o