P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders
| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-01-01
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| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774424006563 |
| _version_ | 1797267443035406336 |
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| author | Ayda Abolhassani Zohreh Fattahi Maryam Beheshtian Mahsa Fadaee Raheleh Vazehan Fatemeh Ahangari Shima Dehdahsi Mehrshid Faraji Zonooz Elham Parsimehr Zahra Kalhor Fatemeh Peymani Maryam Mozaffarpour Nouri Mojgan Babanejad Khadijeh Noudehi Fatemeh Fatehi Shima Zamanian Najafabadi Fariba Afroozan Hilda Yazdan Bita Bozorgmehr Azita Azarkeivan Shokouh Sadat Mahdavi Pooneh Nikuei Farzad Fatehi Payman Jamali Mahmoud Reza Ashrafi Parvaneh Karimzadeh Haleh Habibi Kimia Kahrizi Shahriar Nafissi Ariana Kariminejad Hossein Najmabadi |
| author_facet | Ayda Abolhassani Zohreh Fattahi Maryam Beheshtian Mahsa Fadaee Raheleh Vazehan Fatemeh Ahangari Shima Dehdahsi Mehrshid Faraji Zonooz Elham Parsimehr Zahra Kalhor Fatemeh Peymani Maryam Mozaffarpour Nouri Mojgan Babanejad Khadijeh Noudehi Fatemeh Fatehi Shima Zamanian Najafabadi Fariba Afroozan Hilda Yazdan Bita Bozorgmehr Azita Azarkeivan Shokouh Sadat Mahdavi Pooneh Nikuei Farzad Fatehi Payman Jamali Mahmoud Reza Ashrafi Parvaneh Karimzadeh Haleh Habibi Kimia Kahrizi Shahriar Nafissi Ariana Kariminejad Hossein Najmabadi |
| author_sort | Ayda Abolhassani |
| collection | DOAJ |
| first_indexed | 2024-04-25T01:16:40Z |
| format | Article |
| id | doaj.art-2b6cd8a2516d4c7dba834e7f5dd8bf1b |
| institution | Directory Open Access Journal |
| issn | 2949-7744 |
| language | English |
| last_indexed | 2024-04-25T01:16:40Z |
| publishDate | 2024-01-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Genetics in Medicine Open |
| spelling | doaj.art-2b6cd8a2516d4c7dba834e7f5dd8bf1b2024-03-09T09:32:53ZengElsevierGenetics in Medicine Open2949-77442024-01-012101510P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disordersAyda Abolhassani0Zohreh Fattahi1Maryam Beheshtian2Mahsa Fadaee3Raheleh Vazehan4Fatemeh Ahangari5Shima Dehdahsi6Mehrshid Faraji Zonooz7Elham Parsimehr8Zahra Kalhor9Fatemeh Peymani10Maryam Mozaffarpour Nouri11Mojgan Babanejad12Khadijeh Noudehi13Fatemeh Fatehi14Shima Zamanian Najafabadi15Fariba Afroozan16Hilda Yazdan17Bita Bozorgmehr18Azita Azarkeivan19Shokouh Sadat Mahdavi20Pooneh Nikuei21Farzad Fatehi22Payman Jamali23Mahmoud Reza Ashrafi24Parvaneh Karimzadeh25Haleh Habibi26Kimia Kahrizi27Shahriar Nafissi28Ariana Kariminejad29Hossein Najmabadi30Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran, Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranGenetic Clinic of Tehran Welfare Organization, Tehran, IranMolecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran, Nasle Salem Genetic Counseling Center, Bandar Abbas, IranDepartment of Neurology, Neuromuscular Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran, IranGenetic Counseling Center, Shahroud Welfare Organization, Semnan, IranChildren’s Medical Center, Tehran University of Medical Sciences, Tehran, IranPediatric Neurology Department, Shahid Beheshti University of Medical Sciences, Tehran, IranHamedan University of Medical Science, Hamedan, IranGenetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, IranDepartment of Neurology, Neuromuscular Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, IranKariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran, Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iranhttp://www.sciencedirect.com/science/article/pii/S2949774424006563 |
| spellingShingle | Ayda Abolhassani Zohreh Fattahi Maryam Beheshtian Mahsa Fadaee Raheleh Vazehan Fatemeh Ahangari Shima Dehdahsi Mehrshid Faraji Zonooz Elham Parsimehr Zahra Kalhor Fatemeh Peymani Maryam Mozaffarpour Nouri Mojgan Babanejad Khadijeh Noudehi Fatemeh Fatehi Shima Zamanian Najafabadi Fariba Afroozan Hilda Yazdan Bita Bozorgmehr Azita Azarkeivan Shokouh Sadat Mahdavi Pooneh Nikuei Farzad Fatehi Payman Jamali Mahmoud Reza Ashrafi Parvaneh Karimzadeh Haleh Habibi Kimia Kahrizi Shahriar Nafissi Ariana Kariminejad Hossein Najmabadi P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders Genetics in Medicine Open |
| title | P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders |
| title_full | P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders |
| title_fullStr | P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders |
| title_full_unstemmed | P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders |
| title_short | P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders |
| title_sort | p604 diagnostic utility of ngs testing in a highly consanguineous population findings from 1400 iranian patients with mendelian disorders |
| url | http://www.sciencedirect.com/science/article/pii/S2949774424006563 |
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