karyotype in A Sentence

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    In a male affected with Down syndrome, it results in a Karyotype of 46XY, t14q21q.

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    Testicular feminisation: also called androgen resistance syndrome, this occurs with an XY Karyotype.

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    This Karyotype was found in a 24-year-old man who had signs of Klinefelter syndrome.

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    This Karyotype was found in a 24-year-old man who had signs of KS.

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    To confirm mosaicism, analysis of the Karyotype using dermal fibroblasts or testicular tissue is also possible.

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    With the discovery of Karyotype techniques in the 1950s, it became possible to identify abnormalities of chromosomal number or shape.

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    So the Karyotype of most women is said to be 46,XX and the Karyotype of most men is said to be 46,XY.

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    A coarctation of the aorta in a female is suggestive of Turner syndrome and suggests the need for further tests, such as a Karyotype.

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    The first published report of a man with a 47,XXY Karyotype was by Patricia Jacobs and John Strong at Western General Hospital in Edinburgh, Scotland, in 1959.

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    Analogous XXY syndromes are known to occur in cats-specifically, the presence of calico or tortoiseshell markings in male cats is an indicator of the relevant abnormal Karyotype.

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    The first published report of a female with a 45,X Karyotype was in 1959 by Dr. Charles Ford and colleagues in Harwell, Oxfordshire and Guy's Hospital in London.

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    The first published report of a female with a 45,X Karyotype was in 1959 by Dr. Charles Ford and colleagues in Harwell near Oxford, and Guy's Hospital in London.

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    Those who have one child with Down syndrome have about a 1% risk of having a second child with the syndrome, if both parents are found to have normal Karyotypes.

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    Considering other Karyotype groups, though, they reported a prevalence of 24.3% and 11% in people with mosaic X monosomy, and a rate of 11% in people with X chromosomal structural abnormalities.

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    While XXY males can possibly be characterised based on physical characteristics, substantial variation in physical and developmental traits mean the only reliable method of positive or negative identification is Karyotype testing.

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    While XXY klinefelter can possibly be characterised based on physical characteristics, substantial variation in physical and developmental traits mean the only reliable method of positive or negative identification is Karyotype testing.

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    While some women with Turner syndrome have successfully become pregnant and carried their pregnancies to term, this is very rare and is generally limited to those women whose Karyotypes are not 45, X.

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    The symptoms of KS are often variable; therefore, a Karyotype analysis should be ordered when small testes, infertility, gynecomastia, long arms/legs, developmental delay, speech/language deficits, learning disabilities/academic issues, and/or behavioral issues are present in an individual.

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    The fetuses diagnosed through positive maternal serum screening are more often found to have a mosaic Karyotype than those diagnosed based on ultrasonographic abnormalities, and conversely, those with mosaic Karyotypes are less likely to have associated ultrasound abnormalities.

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