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Pediatrics|January 22, 2014
Mortality and morbidity of VLBW infants with trisomy 13 or trisomy 18Nansi S Boghossian, Nellie I Hansen, Edward F Bell, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.
Medrxiv : the Preprint Server for Health Sciences|December 23, 2024
Multi-ancestry Genome Wide Association Study Meta-analysis of Non-syndromic Orofacial CleftsZhonglin Jia, Nandita Mukhopadhyay, Zhenglin Yang, et al.
Nature Genetics|September 10, 2002
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromesShinji Kondo, Brian C Schutte, Rebecca J Richardson, et al.
Human Molecular Genetics|September 26, 2009
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palateLina M Moreno, Maria Adela Mansilla, Steve A Bullard, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Is 7p14.1 an orofacial cleft risk locus? Genome-wide study of copy number variation in multiple populations provides both a replication of previous studies and an alternative explanationNandita Mukhopadhyay, Eleanor E Feingold, Harrison Brand, et al.
American Journal of Human Genetics|June 24, 2020
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft TriosMadison R Bishop, Kimberly K Diaz Perez, Miranda Sun, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 12, 2021
Genome-Wide Scan for Parent-of-Origin Effects in a sub-Saharan African Cohort With Nonsyndromic Cleft Lip and/or Cleft Palate (CL/P)Lord J J Gowans, Carissa L Comnick, Peter A Mossey, et al.
Human Molecular Genetics|January 17, 2020
SPECC1L regulates palate development downstream of IRF6Everett G Hall, Luke W Wenger, Nathan R Wilson, et al.
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