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American Journal of Medical Genetics. Part A|March 28, 2013
Familial microdeletion of 17q24.3 upstream of SOX9 is associated with isolated Pierre Robin sequence due to position effectIna E Amarillo, Katrina M Dipple, Fabiola Quintero-Rivera
Journal of Pediatric Genetics|November 30, 2016
Genetic Screening in Patients with Craniofacial MalformationsAmanda J Yoon, Binh N Pham, Katrina M Dipple
Alcoholism, Clinical and Experimental Research|May 25, 2016
Alcohol Intervention for Adolescents with Fetal Alcohol Spectrum Disorders: Project Step Up, a Treatment Development StudyMary J O'Connor, Justin Quattlebaum, Marleen Castañeda, et al.
Case Reports in Genetics|October 18, 2012
Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysisOmid Kohannim, Jane Peredo, Katrina M Dipple, et al.
Clinical Dysmorphology|September 13, 2005
Duplication of the Down syndrome critical region does not predict facial phenotype in a baby with a ring chromosome 21Eric A Crombez, Katrina M Dipple, Lisa A Schimmenti, et al.
Pediatrics|December 29, 2020
Management Principles for Acute Illness in Patients With Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyTracy L McGregor, Susan A Berry, Katrina M Dipple, et al.
Birth Defects Research|January 25, 2019
Suicide risk in adolescents with fetal alcohol spectrum disordersMary J O'Connor, Larissa C Portnoff, Michael Lebsack-Coleman, et al.
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