Showing results (1-10 of 9) with videos related to
Sort By:
Pageof 1
American Journal of Medical Genetics|May 1, 1989
Wisconsin consanguinity studies. II: Familial adenocarcinomatosisR R Lebel, W B GallagherAmerican Journal of Medical Genetics|August 1, 1983
Consanguinity studies in Wisconsin I: secular trends in consanguineous marriage, 1843-1981R R LebelArchives of Surgery (Chicago, Ill. : 1960)|March 1, 1977
Paraganglioma simulating primary rib tumorJ J Smalley, W B Gallagher, C P NicholsAmerican Journal of Medical Genetics|August 3, 2001
Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and reviewM L Leonardi, G S Pai, B Wilkes, et al.Clinical Genetics|April 10, 2002
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 geneR R Lebel, M May, S Pouls, et al.Wisconsin Medical Journal|February 1, 1994
DNA testing and genetic counseling: truth or consequencesN C Reynolds, R R Lebel, K de S Hamsher, et al.American Journal of Medical Genetics|April 1, 1984
Tandem dup (1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomaliesB R Elejalde, J M Opitz, M M de Elejalde, et al.Human Molecular Genetics|February 1, 1996
Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.Clinical Genetics|April 23, 2016
Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotypingJ S Amos, L Huang, J Thevenon, et al.Pageof 1