Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients

Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients

In this study, nineteen cases of suspected or clinically diagnosed Prader-Willi Syndrome (PWS) were tested for molecular deletions by in situ hybridization with two DNA probes, IR4-3R and GABRB3. Both probes are specific for sequences within the chromosome region 15q11-13, with IR4-3R located withi...

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Bibliographic Details
Main Author: Robinett, Sheldon J. (Sheldon Jay)
Format: Others
Language:English
Published: University of North Texas 1994
Subjects:
Prader-Willi Syndrome
Angelman Syndrome
genomic imprinting
Online Access:https://digital.library.unt.edu/ark:/67531/metadc332745/
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spelling ndltd-unt.edu-info-ark-67531-metadc3327452017-07-14T05:27:28Z Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients Robinett, Sheldon J. (Sheldon Jay) Prader-Willi Syndrome Angelman Syndrome genomic imprinting In this study, nineteen cases of suspected or clinically diagnosed Prader-Willi Syndrome (PWS) were tested for molecular deletions by in situ hybridization with two DNA probes, IR4-3R and GABRB3. Both probes are specific for sequences within the chromosome region 15q11-13, with IR4-3R located within the putative PWS region and GABRB3 in the distal area associated with Angelman Syndrome. University of North Texas 1994-12 Thesis or Dissertation Text local-cont-no: 1002720534-Robinett https://digital.library.unt.edu/ark:/67531/metadc332745/ ark: ark:/67531/metadc332745 English Public ... Copyright Copyright is held by the author, unless otherwise noted. All rights reserved.
collection NDLTD
language English
format Others
sources NDLTD
topic Prader-Willi Syndrome
Angelman Syndrome
genomic imprinting
spellingShingle Prader-Willi Syndrome
Angelman Syndrome
genomic imprinting
Robinett, Sheldon J. (Sheldon Jay)
Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
description In this study, nineteen cases of suspected or clinically diagnosed Prader-Willi Syndrome (PWS) were tested for molecular deletions by in situ hybridization with two DNA probes, IR4-3R and GABRB3. Both probes are specific for sequences within the chromosome region 15q11-13, with IR4-3R located within the putative PWS region and GABRB3 in the distal area associated with Angelman Syndrome.
author Robinett, Sheldon J. (Sheldon Jay)
author_facet Robinett, Sheldon J. (Sheldon Jay)
author_sort Robinett, Sheldon J. (Sheldon Jay)
title Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
title_short Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
title_full Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
title_fullStr Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
title_full_unstemmed Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
title_sort genomic imprinting: support for the concept from a study of prader-willi syndrome patients
publisher University of North Texas
publishDate 1994
url https://digital.library.unt.edu/ark:/67531/metadc332745/
work_keys_str_mv AT robinettsheldonjsheldonjay genomicimprintingsupportfortheconceptfromastudyofpraderwillisyndromepatients
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