Zobrazeno 1 - 10
of 26
pro vyhledávání: '"J T, Mascarello"'
Publikováno v:
Cytogenetic and Genome Research. 86:194-203
The physical and genetic characterization of a stable human minichromosome in a Chinese hamster hybrid cell is described. The minichromosome is 2–3 Mb in size, is linear, and contains a complementing SDHC gene. It is derived from a human chromosome
High incidence of XXY and XYY males among the offspring of female chimeras from embryonic stem cells
Publikováno v:
Scopus-Elsevier
Injecting male embryonic stem cells into the blastocoel of female embryos occasionally produces female chimeras capable of transmitting the embryonic stem cell genome. In our experiments several embryonic stem cell-derived male offspring from female
Publikováno v:
Prenatal Diagnosis. 14:163-165
We report the detection of a mosaic triple trisomy, 46, XY/49, XY, + 13, +20, +21, in two amniotic fluid specimens obtained from a pregnancy that yielded a normal infant. Traditional cytogenetic methods failed to detect the abnormal cell lineage in f
Autor:
L M, Bird, J T, Mascarello
Publikováno v:
American journal of medical genetics. 100(1)
A patient with dir dup 2(q37.1q33.1) is described. Literature review of chromosome 2q duplications suggests a consistent, though nonspecific, facial phenotype. Segregation of those cases that are "pure" duplications from those with accompanying monos
Publikováno v:
Cytogenetics and cell genetics. 86(3-4)
The physical and genetic characterization of a stable human minichromosome in a Chinese hamster hybrid cell is described. The minichromosome is 2-3 Mb in size, is linear, and contains a complementing SDHC gene. It is derived from a human chromosome 1
Publikováno v:
American journal of medical genetics. 70(1)
A female patient with the karyotype 45,X/46, X, r(X)(p11.2 q13) and severe developmental delay, prominent fingertip pads, long palpebral fissures, short stature, and history of hypotonia had a phenotype reminiscent of Kabuki syndrome. We hypothesized
Publikováno v:
Journal of Investigative Medicine. 53:S135.5-S135
The karyotype 46,X,isodicentric Y has rarely been reported in the context of prenatal diagnosis. The literature, however, is replete with descriptions of individuals who are 46,X isodicentric Y/45,X, presenting with a spectrum of phenotypes from Turn
Publikováno v:
Journal of Mammalogy. 55:831-834
Publikováno v:
Journal of Mammalogy. 55:695-704
The Giemsa banding pattern of the karyotype of Neotoma micropus is compared with the banding patterns of seven other rodent species that are progressively more distantly related to N. micropus . Results of comparisons imply that there is a tendency f
Autor:
Ronald V. Lacro, Kenneth Lyons Jones, J. T. Mascarello, Oliver W. Jones, Nevin Wilson, Marilyn C. Jones, James F. Reynolds
Publikováno v:
American Journal of Medical Genetics. 26:719-728
Four children and one spontaneously aborted fetus from 2 separate families have a similar pattern of malformation secondary to duplication of distal 15q. In both families, the abnormal chromosomes were derived from balanced reciprocal translocations