Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Neurology|April 1, 1998
Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)A Gambardella, A Bolino, M Muglia, et al.
American Journal of Medical Genetics|June 8, 2001
Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndromeI D Krantz, E Tonkin, M Smith, et al.
Revista De Neurologia|May 15, 1998
[Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage]M Arcos-Burgos, L G Palacio, I Jiménez, et al.
Alimentary Pharmacology & Therapeutics|January 31, 2006
Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitisO Palmieri, A Latiano, R Valvano, et al.
International Journal of Molecular Medicine|December 15, 2000
Exclusion of candidate genes and chromosomal regions in familial neuroblastomaG P Tonini, C McConville, R Cusano, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2C Lo Nigro, R Cusano, M Scaranari, et al.
Human Genetics|December 18, 1998
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patientsM C Rosatelli, A Meloni, A Meloni, et al.
Lancet (London, England)|May 10, 1997
Polymorphisms of alpha-adducin and salt sensitivity in patients with essential hypertensionD Cusi, C Barlassina, T Azzani, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Pageof 8