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American Journal of Medical Genetics. Part A|November 2, 2011
A de novo 2.1-Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic featuresVazken M Der Kaloustian, Laura Russell, Swaroop Aradhya, et al.The Journal of Investigative Dermatology|March 11, 2006
A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosisKelly A McGowan, Swaroop Aradhya, Helmut Fuchs, et al.Genomics|August 6, 2002
The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autismTakanori Yamagata, Swaroop Aradhya, Masato Mori, et al.Reproductive Biomedicine Online|February 12, 2025
Derivative and non-derivative aneuploidy rates in PGT tested blastocysts from carriers of structural rearrangementsLauren Walters-Sen, Dana Neitzel, Rachel E Ellsworth, et al.American Journal of Medical Genetics. Part A|March 16, 2013
Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndromeMohamed Khalifa, Jennifer Stein, Lance Grau, et al.Journal of Pediatric Hematology/Oncology|September 11, 2010
A pediatric B lineage leukemia with coincident MYC and MLL translocationsNathan D Meeker, Athena M Cherry, Charles D Bangs, et al.American Journal of Medical Genetics. Part A|August 19, 2004
Mild developmental delay in terminal chromosome 6p deletionKelly M Chen, Athena M Cherry, Jin S Hahn, et al.Adolescent Medicine (Philadelphia, Pa.)|May 3, 2002
FISHing for answers: the use of molecular cytogenetic techniques in adolescent medicine practiceRuth J Lin, Athena M Cherry, Charles D Bangs, et al.American Journal of Obstetrics and Gynecology|March 27, 2013
Is it time to sound an alarm about false-positive cell-free DNA testing for fetal aneuploidy?Michael T Mennuti, Athena M Cherry, Jennifer J D Morrissette, et al.Frontiers in Immunology|June 27, 2022
Global Expansion of Jeffrey's Insights: Jeffrey Modell Foundation's Genetic Sequencing Program for Primary ImmunodeficiencyJessica Quinn, Vicki Modell, Britt Johnson, et al.Pageof 13