Human Genome Epidemiology Literature Finder
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| Query Trace: Syndrome and QRICH2[original query] |
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| Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Clinical genetics 2019 Jul . Kherraf Zine-Eddine, Cazin Caroline, Coutton Charles, Amiri-Yekta Amir, Martinez Guillaume, Boguenet Magalie, Fourati Ben Mustapha Selima, Kharouf Mahmoud, Gourabi Hamid, Hosseini Seyedeh Hanieh, Daneshipour Abbas, Touré Aminata, Thierry-Mieg Nicolas, Zouari Raoudha, Arnoult Christophe, Ray Pierre |
- Page last reviewed:Feb 1, 2024
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