Zobrazeno 1 - 10
of 20
pro vyhledávání: '"J R, Byrd"'
Publikováno v:
Clinical Genetics. 34:74-78
A case of an infant with ring chromosome 5 is presented. The phenotype of this patient and other reported cases is analyzed with respect to the deletion of the long arm of chromosome 5.
Publikováno v:
Journal of Medical Genetics. 27:137-138
Autor:
P G, McDonough, J R, Byrd
Publikováno v:
Clinical Obstetrics and Gynecology. 20:565-579
The spectrum of patients with gonadal dysgenesis has expanded over the last decade to include cytogenetically normal individuals. Comprehension of the etiology of gonadal maldevelopment in these patients remains tenuous. More careful study of pedigre
Publikováno v:
Fertility and sterility. 38(6)
Publikováno v:
Obstetrics and gynecology. 54(5)
Eight documented cases of true hermaphroditism have been seen in the reproductive endocrine unit at the Medical College of Georgia since 1969. There was histologic evidence of both ovarian and testicular tissue in all cases. Seven patients had periph
Publikováno v:
Journal of the National Medical Association. 73(8)
Evidence is presented that the vinca alkaloids (vinblastine, vincristine, and vindesine) exert an immunopotentiating effect on the antibody response to sheep red blood cells (SRBC). The primary antibody response, measured by the rosette-forming cell
Publikováno v:
Fertility and sterility. 34(3)
The cytogenetic and phenotypic findings in 15 patients with 45,X/46,XY mosaicism are described. Six patients presented with delayed sexual development without masculinization. The remaining nine patients had varying degrees of masculinization, rangin
Publikováno v:
Fertility and sterility. 32(4)
From 1958 through 1977, 100 couples with documented recurrent reproductive failure were evaluated in the reproductive endocrine unit of the Medical College of Georgia. All couples underwent cytogenetic studies, radiologic evaluation of the Müllerian
Publikováno v:
Obstetrics and gynecology. 47(3)
Gonadoblastomas arise in dysgenetic gonads of individual possessing a Y chromosome in their karyotype. This is the first report of a gonadoblastoma in a 46,XX true hermaphrodite.
Publikováno v:
Obstetrics and gynecology. 47(3)
Determinations of multiple steroids were made on ovarian and peripheral blood in a 46,XY patient with bilateral gonadoblastoma. The right gonadoblastoma had undergone complete calcific ablation. The principal viable cellular elements in the left gona