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The New England Journal of Medicine|July 8, 1982
Myelomatosis with type III hyperlipoproteinemia: clinical and metabolic studiesC Cortese, B Lewis, N E Miller, et al.
Der Radiologe|January 23, 2016
[Quantitative perfusion imaging in magnetic resonance imaging]F G Zöllner, T Gaa, F Zimmer, et al.
American Journal of Human Genetics|March 26, 1999
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration?M Krings, A E Salem, K Bauer, et al.
Clinical Genetics|June 30, 2010
Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysisV Grossmann, M Höckner, H Karmous-Benailly, et al.
Clinical Genetics|October 15, 2013
Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomaliesA Spreiz, E Haberlandt, M Baumann, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndromeA Silahtaroglu, F A Hol, P K Jensen, et al.
American Journal of Human Genetics|March 21, 2000
Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndromeM Witsch-Baumgartner, B U Fitzky, M Ogorelkova, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 11, 2021
Asymptomatic SARS-CoV-2 infection: A systematic review and meta-analysisPratha Sah, Meagan C Fitzpatrick, Charlotte F Zimmer, et al.
Journal of the American Veterinary Medical Association|August 1, 1986
Portosystemic shunts in cats: seven cases (1976-1984)T D Scavelli, W E Hornbuckle, L Roth, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutationsM Witsch-Baumgartner, E Ciara, J Löffler, et al.
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