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Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease |
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Title: |
Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease |
Author: |
Malhotra, Alka Thorpe, Erin Coffey, Alison J. Rajkumar, Revathi Adjeman, Josephine Naa Adjeley Adjetey, Naomi Dianne Aglobitse, Sharron Allotey, Felix Arsov, Todor Ashong, Joyce Badoe, Ebenezer Vincent Basel, Donald Brew, Yvonne Brown, Chester Bosfield, Kerri Casas, Kari Cornejo-Olivas, Mario Davis-Keppen, Laura Freed, Abbey Gibson, Kate Jayakar, Parul Jones, Marilyn C. Kawome, Martina Lumaka, Aimé Maier, Ursula Makay, Prince Manassero, Gioconda Marbell-Wilson, Marilyn Marcuccilli, Charles Masser-Frye, Diane McCarrier, Julie Mills, Hannah-Sharon Montoya, Jeny Balazar Mubungu, Gerrye Ngole, Mamy Perez, Jorge Pivnick, Eniko Duenas-Roque, Milagros M. Pena Salguero, Hildegard Serize, Arturo Shinawi, Marwan Sirchia, Fabio Soler-Alfonso, Claudia Taylor, Alan Thompson, Lauren Vance, Gail Vanderver, Adeline Vaux, Keith Velasco, Danita Wiafe, Samuel Taft, Ryan J. Perry, Denise L. Kesari, Akanchha |
Appeared in: |
Human genetics and genomics advances |
Paging: |
Volume 6 () nr. 3 pages p. |
Year: |
2025 |
Contents: |
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Publisher: |
The Authors |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
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