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American Journal of Medical Genetics. Part A|February 16, 2018
De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomaliesHailey Pinz, Louise C Pyle, Dong Li, et al.
Plos One|October 19, 2019
Birth outcomes in women who have taken adalimumab in pregnancy: A prospective cohort studyChristina D Chambers, Diana L Johnson, Ronghui Xu, et al.
Arthritis and Rheumatism|February 5, 2010
Birth outcomes in women who have taken leflunomide during pregnancyChristina D Chambers, Diana L Johnson, Luther K Robinson, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|November 2, 2021
Birth Outcomes in Women Who Have Taken Hydroxycholoroquine During Pregnancy: A Prospective Cohort StudyChristina D Chambers, Diana L Johnson, Ronghui Xu, et al.
American Journal of Medical Genetics. Part A|April 3, 2008
Development and validation of a measure of dysmorphology: useful for autism subgroup classificationJudith H Miles, T Nicole Takahashi, Julie Hong, et al.
Orphanet Journal of Rare Diseases|March 19, 2020
Abnormally increased carotid intima media-thickness and elasticity in patients with Morquio A diseaseRaymond Y Wang, Kyle D Rudser, Donald R Dengel, et al.
The Journal of Pediatrics|July 22, 2017
Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15-Month ExperienceBarbara K Burton, Joel Charrow, George E Hoganson, et al.
Human Mutation|February 12, 2019
Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2Ellen F Macnamara, Alanna E Koehler, Precilla D'Souza, et al.
International Journal of Neonatal Screening|October 19, 2020
Newborn Screening for Pompe Disease in Illinois: Experience with 684,290 InfantsBarbara K Burton, Joel Charrow, George E Hoganson, et al.
Journal of Medical Genetics|July 18, 2015
Mutations in COQ4, an essential component of coenzyme Q biosynthesis, cause lethal neonatal mitochondrial encephalomyopathyWendy K Chung, Kimberly Martin, Chaim Jalas, et al.
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