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Clinical Genetics|June 4, 1998
Maternal cell contamination of buccal smear samples in nursing neonatesD Babovic-Vuksanovic, V V Michels, M E Law, et al.Sensors (Basel, Switzerland)|April 13, 2024
A Vehicle-Edge-Cloud Framework for Computational Analysis of a Fine-Tuned Deep Learning ModelM Jalal Khan, Manzoor Ahmed Khan, Sherzod Turaev, et al.American Journal of Medical Genetics|December 26, 2001
Tandem translocation of chromosomes 22 and 15 with two preserved satellite stalk regions and deletion 22q13.3-qterK A Lee, S H Kim, M H Lee, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2011
Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridizationBrandon M Shearer, Erik C Thorland, Austin W Carlson, et al.American Journal of Medical Genetics. Part A|April 6, 2005
Subtelomere deletions and translocations are frequently familialAdewale Adeyinka, S Annie Adams, Cindy P Lorentz, et al.Journal of Medical Genetics|February 1, 1978
Trisomy 18 syndrome with an unusual karyotype: possible double isochromosomeL M Larson, W A Wasdahl, J H Saumur, et al.Bioelectrochemistry (Amsterdam, Netherlands)|November 14, 2017
On-chip signal amplification of magnetic bead-based immunoassay by aviating magnetic bead chainsUddin M Jalal, Gyeong Jun Jin, Kyu Shik Eom, et al.JPMA. the Journal of the Pakistan Medical Association|November 26, 2008
Kikuchi-Fujimoto Disease presenting with fever, lymphadenopathy and dysphagiaA K M Mosharraf-Hossain, Pran Gopal Datta, A S Ahmed Amin, et al.Prenatal Diagnosis|March 1, 2000
Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmationJ L Hand, V V Michels, M J Marinello, et al.Annales De Genetique|January 1, 1988
Complete trisomy 17p a relatively new syndromeJ T Martsolf, L Larson, S M Jalal, et al.Pageof 18