Cargando…

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

Detalles Bibliográficos
Autores principales: Demir, Korcan, Nalbantoğlu, Özlem, Karaer, Kadri, Korkmaz, Hüseyin Anıl, Yıldız, Melek, Tunç, Selma, Özkan, Behzat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805220/
https://www.ncbi.nlm.nih.gov/pubmed/26777052
http://dx.doi.org/10.4274/jcrpe.2597
_version_ 1782423113433088000
author Demir, Korcan
Nalbantoğlu, Özlem
Karaer, Kadri
Korkmaz, Hüseyin Anıl
Yıldız, Melek
Tunç, Selma
Özkan, Behzat
author_facet Demir, Korcan
Nalbantoğlu, Özlem
Karaer, Kadri
Korkmaz, Hüseyin Anıl
Yıldız, Melek
Tunç, Selma
Özkan, Behzat
author_sort Demir, Korcan
collection PubMed
description
format Online
Article
Text
id pubmed-4805220
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Galenos Publishing
record_format MEDLINE/PubMed
spelling pubmed-48052202016-04-06 Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy Demir, Korcan Nalbantoğlu, Özlem Karaer, Kadri Korkmaz, Hüseyin Anıl Yıldız, Melek Tunç, Selma Özkan, Behzat J Clin Res Pediatr Endocrinol Letter to Editor Galenos Publishing 2015-12 2015-12-03 /pmc/articles/PMC4805220/ /pubmed/26777052 http://dx.doi.org/10.4274/jcrpe.2597 Text en © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to Editor
Demir, Korcan
Nalbantoğlu, Özlem
Karaer, Kadri
Korkmaz, Hüseyin Anıl
Yıldız, Melek
Tunç, Selma
Özkan, Behzat
Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
title Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
title_full Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
title_fullStr Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
title_full_unstemmed Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
title_short Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
title_sort genetic diagnosis using whole exome analysis in two cases with malignant osteopetrosis of infancy
topic Letter to Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805220/
https://www.ncbi.nlm.nih.gov/pubmed/26777052
http://dx.doi.org/10.4274/jcrpe.2597
work_keys_str_mv AT demirkorcan geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy
AT nalbantogluozlem geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy
AT karaerkadri geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy
AT korkmazhuseyinanıl geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy
AT yıldızmelek geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy
AT tuncselma geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy
AT ozkanbehzat geneticdiagnosisusingwholeexomeanalysisintwocaseswithmalignantosteopetrosisofinfancy