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Pediatric Research|November 14, 1997
Increased leptin messenger RNA and serum leptin levels in children with Prader-Willi syndrome and nonsyndromal obesityA C Lindgren, C Marcus, C Skwirut, et al.Human Genetics|August 1, 1988
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyriaJ S Lee, M Anvret, J Lindsten, et al.American Journal of Human Genetics|May 1, 1994
Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromesA Reis, B Dittrich, V Greger, et al.Human Genetics|February 1, 1994
394delTT: a Nordic cystic fibrosis mutationM Schwartz, M Anvret, M Claustres, et al.American Journal of Medical Genetics|December 20, 2000
NURR1 mutations in cases of schizophrenia and manic-depressive disorderS Buervenich, A Carmine, M Arvidsson, et al.Journal of Medical Genetics|December 1, 1995
Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyriaG Lundin, J Hashemi, Y Floderus, et al.Journal of Pathology Informatics|January 31, 2024
Use of n-grams and K-means clustering to classify data from free text bone marrow reportsRichard F XiangJournal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.Genomics|November 1, 1989
Recombination events that locate myotonic dystrophy distal to APOC2 on 19qK Johnson, P Shelbourne, J Davies, et al.Journal of Virology|October 9, 1999
The trophoblastic epithelial barrier is not infected in full-term placentae of human immunodeficiency virus-seropositive mothers undergoing antiretroviral therapyC Tscherning-Casper, N Papadogiannakis, M Anvret, et al.Pageof 18