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Human Genetics|January 1, 1984
Localisation of genetic markers and orientation of the linkage group on chromosome 19J D Brook, D J Shaw, L Meredith, et al.Journal of Medical Genetics|August 1, 1983
Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosomeH M Kingston, N S Thomas, P L Pearson, et al.American Journal of Human Genetics|January 1, 1989
Close flanking markers for neurofibromatosis type I (NF1)M Upadhyaya, M Sarfarazi, S M Huson, et al.Archives of Disease in Childhood|April 1, 1992
Anal abnormalities in childhood myotonic dystrophy--a possible source of confusion in child sexual abuseW Reardon, H E Hughes, S H Green, et al.The Journal of Pediatrics|March 1, 1989
Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysisJ Zonana, M Sarfarazi, N S Thomas, et al.Pediatric Pulmonology|May 17, 2012
Electromagnetic inductance plethysmography to measure tidal breathing in preterm and term infantsN Pickerd, E M Williams, S KotechaJournal of Applied Behavior Analysis|March 13, 2023
Some effects of detection dogs on passenger behavior at border control portsEmma E M Williams, Rebecca A SharpThe Quarterly Journal of Medicine|June 1, 1991
Polycystic kidney disease re-evaluated: a population-based studyF Davies, G A Coles, P S Harper, et al.Prenatal Diagnosis|September 1, 1990
Chorionic villus sampling for prenatal diagnosis in Wales using DNA probes--5 years' experienceM Upadhyaya, A Fryer, G Foat, et al.Journal of Neurology|June 15, 1999
Daytime somnolence in myotonic dystrophyM F Phillips, H M Steer, J R Soldan, et al.Pageof 30