Analysis of D/D translocations in man by differential staining

With the advent of new cytogenetic techniques, more questions can be answered concerning chromosomal rearrangements. The questions considered in this study ask which chromosomes are involved in the t(Dq Dq) translocation, where are the break points located, and what are the possible mechanisms of...

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Main Author: Wilson, Robert Douglas
Language:English
Published: 2010
Online Access:http://hdl.handle.net/2429/19349
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-193492018-01-05T17:39:55Z Analysis of D/D translocations in man by differential staining Wilson, Robert Douglas With the advent of new cytogenetic techniques, more questions can be answered concerning chromosomal rearrangements. The questions considered in this study ask which chromosomes are involved in the t(Dq Dq) translocation, where are the break points located, and what are the possible mechanisms of t(Dq Dq) translocation formation. The segregation pattern of the D/D translocation was considered when the chromosome translocation was shown to be familial. Chromosomes were obtained from leukocyte blood cultures and three differential staining techniques (Giemsa-banding, fluorescent-banding, C-banding) were used to identify the chromosomes involved in the D/D translocation. These techniques also allowed the break points in each chromosome to be estimated. Four families and a single spontaneous case were examined. The segregation pattern of the t(Dq Dq) translocation was discussed for the familial translocations. The possible mechanisms of formation of these D/D translocations was also discussed. The cytogenetic investigation revealed these general results . 1. A homologous t(14q;14q) chromosome, which appeared to be monocentric, was found in a male infant who was ascertained through an investigation of his short stature. 2. A homologous t(13q;13q) chromosome, which appeared to be dicentric, was found in a family who was ascertained through the birth of a male with numerous congenital malformations. 3. A t(13q;14q) translocation chromosome, which appeared to be dicentric, was found in a family who was ascertained through the birth of a mentally retarded male. 4. A t(13q;14q) translocation chromosome, which appeared to be monocentric, was found in a family who was ascertained through the birth of a mentally retarded male. 5. A t(13q;14q) translocation chromosome and a t(13p;14p) translocation chromosome was found in a family who was ascertained through the birth of a mentally retarded male. Medicine, Faculty of Medical Genetics, Department of Graduate 2010-01-29T20:36:26Z 2010-01-29T20:36:26Z 1974 Text Thesis/Dissertation http://hdl.handle.net/2429/19349 eng For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.
collection NDLTD
language English
sources NDLTD
description With the advent of new cytogenetic techniques, more questions can be answered concerning chromosomal rearrangements. The questions considered in this study ask which chromosomes are involved in the t(Dq Dq) translocation, where are the break points located, and what are the possible mechanisms of t(Dq Dq) translocation formation. The segregation pattern of the D/D translocation was considered when the chromosome translocation was shown to be familial. Chromosomes were obtained from leukocyte blood cultures and three differential staining techniques (Giemsa-banding, fluorescent-banding, C-banding) were used to identify the chromosomes involved in the D/D translocation. These techniques also allowed the break points in each chromosome to be estimated. Four families and a single spontaneous case were examined. The segregation pattern of the t(Dq Dq) translocation was discussed for the familial translocations. The possible mechanisms of formation of these D/D translocations was also discussed. The cytogenetic investigation revealed these general results . 1. A homologous t(14q;14q) chromosome, which appeared to be monocentric, was found in a male infant who was ascertained through an investigation of his short stature. 2. A homologous t(13q;13q) chromosome, which appeared to be dicentric, was found in a family who was ascertained through the birth of a male with numerous congenital malformations. 3. A t(13q;14q) translocation chromosome, which appeared to be dicentric, was found in a family who was ascertained through the birth of a mentally retarded male. 4. A t(13q;14q) translocation chromosome, which appeared to be monocentric, was found in a family who was ascertained through the birth of a mentally retarded male. 5. A t(13q;14q) translocation chromosome and a t(13p;14p) translocation chromosome was found in a family who was ascertained through the birth of a mentally retarded male. === Medicine, Faculty of === Medical Genetics, Department of === Graduate
author Wilson, Robert Douglas
spellingShingle Wilson, Robert Douglas
Analysis of D/D translocations in man by differential staining
author_facet Wilson, Robert Douglas
author_sort Wilson, Robert Douglas
title Analysis of D/D translocations in man by differential staining
title_short Analysis of D/D translocations in man by differential staining
title_full Analysis of D/D translocations in man by differential staining
title_fullStr Analysis of D/D translocations in man by differential staining
title_full_unstemmed Analysis of D/D translocations in man by differential staining
title_sort analysis of d/d translocations in man by differential staining
publishDate 2010
url http://hdl.handle.net/2429/19349
work_keys_str_mv AT wilsonrobertdouglas analysisofddtranslocationsinmanbydifferentialstaining
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