Search Results - "Rary, J M"

Analysis of Human Y-Chromosome-Specific Reiterated DNA in Chromosome Variants by Kunkel, Louis M., Smith, Kirby D., Boyer, Samuel H., Borgaonkar, Digamber S., Wachtel, Stephen S., Miller, O. J., Breg, W. Roy, Jones, Howard W., Rary, Jack M.

“…A number of individuals with aberrant Y chromosomes have been tested for the presence of Y-chromosome-specific reiterated DNA. These studies locate…”
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The utilization of bromodeoxyuridine incorporation into DNA for the analysis of cellular kinetics by Tice, R, Schneider, E L, Rary, J M

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Double balanced chromosomal translocation carrier (6;8), (13;14)--a case report by Hansen, R G, Anderson, R L, Rary, J M

“…This paper reports the identification of a carrier of two different balanced chromosomal translocations (45,XX,-13,-14, + t(13q;14q), t(6;8) (p11;p12]…”
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G2 chromosomal radiosensitivity in ataxia telangiectasia lymphocytes by Bender, M A, Rary, J M, Kale, R P

“…The peripheral lymphocytes from 7 patients affected with ataxia telangiectasia (AT) were found to be about twice as sensitive to the induction of…”
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Assignment of the H-Y antigen gene to the short arm of chromosome Y by Rary, J M, Cummings, D K, Jones, Jr, H W, Rock, J A

“…We have presented two cases strongly suporting a Y chromosome short-arm location for the H-Y antigen gene. The first case was HY antigen-positive with an…”
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A 14/14 marker chromosome lymphocyte clone in ataxia telangiectasia by Rary, J M, Bender, M A, Kelly, T E

“…A lymphocyte clone with a 45, XY karyotype with a 14/14 tandem translocation marker, the frequency of which is time-variable, has been observed in an ataxia…”
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Cell-cycle duration and sister-chromatid exchange frequency in cultured human lymphocytes by Snope, A J, Rary, J M

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A 5/X chromosomal translocation in a patient with premature menopause by Garcia, J E, Cummings, D K, Wentz, A C, Jones, Jr, H W, Rary, J M

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G2 chromosomal radiosensitivity in Fanconi's anemia by Bigelow, S B, Rary, J M, Bender, M A

“…Both the peripheral lymphocytes from 4 patients affected with the inherited disease Fanconi's anemia (FA), and tissue-culture fibroblasts from skin biopsies…”
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G0 chromosomal radiosensitivity in ataxia telangiectasia lymphocytes by Bender, M A, Rary, J M, Kale, R P

“…Contrary to an earlier report, peripheral lymphocytes from 4 AT patients were not found to exhibit higher yields of unequivocal chromosome type aberrations…”
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Prenatal cytogenetic analysis of women with high risk for genetic disorders by Rary, J M, Park, I J, Heller, R H, Jones, Jr, H W, Baramki, T A

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Variation in chromosome number among European wild pigs by McFee, A F, Banner, M W, Rary, J M

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A (Y;17) translocation in a fibroblast culture from a female with 46 chromosomes. Repository identification No. GM-2598 by Rary, J M, Middleton, A, Mulivor, R A, Greene, A E, Coriell, L L

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Effect of cocultivation on sister chromatid exchange frequencies in Bloom's syndrome and normal fibroblast cells by TICE, R, WINDLER, G, RARY, J. M

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Double balanced chromosomal translocation carrier (6;8), (13;14)--a case report: critique and response by Young, R S

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Current concepts for the surgical management of carotid body tumor by Knight, Theron T., Gonzalez, Jose Andres, Rary, John M., Rush, Daniel S.

“…Carotid body tumor (CBT) is a rare lesion of the neuroendocrine system. Chronic hypoxia has long been recognized as an etiology of CBT and other…”
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Speculation on the role of transposable elements in human genetic disease with particular attention to achondroplasia and the fragile X syndrome by Hoegerman, S F, Rary, J M

“…We suggest that mutations for fragile X-positive Martin-Bell syndrome, and perhaps also for achondroplasia, may result from the insertion of transposable…”
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High spontaneous chromosomal aberration frequency in the cells of an amniotic fluid culture by Rary, J M, Heller, R H

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The fallability of X-chromatin as a screening test for anomalies of the X chromosome by Rary, J M, Cummings, D, Jones, Jr, H W

“…In 13 of 148 patients suspected of anomalies of the X chromosome, the X-chromatin test was misleading. Therefore, if an anomaly is suspected, a karyotype as…”
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The crucial role of fetal age in amniotic fluid interpretation by Bibbins, Jr, P E, Wilds, P L, Jones, Jr, H W, Rary, J M

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