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American Journal of Human Genetics|April 1, 1994
Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5qL van Herwerden, C S Rose, W Reardon, et al.The British Journal of Ophthalmology|May 29, 1998
Optic disc anomalies and frontonasal dysplasiaP Hodgkins, M Lees, J Lawson, et al.Journal of Medical Genetics|September 1, 1996
A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricansD Wilkes, P Rutland, L J Pulleyn, et al.Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.Journal of Medical Genetics|November 1, 1992
Minimal expression of myotonic dystrophy: a clinical and molecular analysisW Reardon, H G Harley, J D Brook, et al.Genomics|December 1, 1991
A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneityW Reardon, H R Middleton-Price, L Sandkuijl, et al.Lancet (London, England)|December 5, 1992
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAW Reardon, R J Ross, M G Sweeney, et al.Lancet (London, England)|May 9, 1992
Unstable DNA sequence in myotonic dystrophyH G Harley, S A Rundle, W Reardon, et al.The British Journal of Ophthalmology|September 1, 1993
Cataract and myotonic dystrophy: the role of molecular diagnosisW Reardon, J C MacMillan, J Myring, et al.Perspectives on Psychological Science : a Journal of the Association for Psychological Science|November 9, 2022
Understanding the Leaders of Tomorrow: The Need to Study Leadership in AdolescenceJennifer L Tackett, Kathleen W Reardon, Nathanael J Fast, et al.Pageof 16