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American Journal of Medical Genetics. Part A|April 9, 2009
A novel SIX3 mutation segregates with holoprosencephaly in a large familyBenjamin D Solomon, Felicitas Lacbawan, Mahim Jain, et al.
Frontiers in Immunology|May 14, 2023
Prediction of HLA genotypes from single-cell transcriptome dataBenjamin D Solomon, Hong Zheng, Laura W Dillon, et al.
The Journal of Pediatrics|February 14, 2018
Clinical, Social, and Genetic Factors Associated with Obesity at 12 Months of AgeSahel Hazrati, Wendy S W Wong, Kathi Huddleston, et al.
Human Genetics|August 16, 2011
Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHHDaniel E Pineda-Alvarez, Erich Roessler, Ping Hu, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and ectrodactyly: Report of three new patients and review of the literatureAmelia A Keaton, Benjamin D Solomon, Anthonie J van Essen, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Deletion of 8q24 in an adult with mild dysmorphic features, developmental delay, and ketotic hypoglycemiaBenjamin D Solomon, Eileen Lange, Jay Shubrook, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literatureEmily F Kauvar, Benjamin D Solomon, Cynthia J R Curry, et al.
Orphanet Journal of Rare Diseases|July 16, 2025
Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionalsBehnam Javanmardi, Rebekah L Waikel, Tinatin Tkemaladze, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Analysis of component findings in 79 patients diagnosed with VACTERL associationBenjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, et al.
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