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B Wirth

Showing results (101-110 of 119) with videos related to

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Human Genetics|November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelicB Wirth, K Zerres, M Fischbach, et al.
Orphanet Journal of Rare Diseases|May 3, 2023
Objective measurement of oral function in adults with spinal muscular atrophyT Kruse, S Shamai, D Leflerovà, et al.
Human Genetics|October 1, 1988
Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)B Wirth, F H Herrmann, M Neugebauer, et al.
American Journal of Nephrology|January 1, 1988
Late manifestation of autosomal-recessive polycystic kidney disease in two sistersH P Neumann, K Zerres, C L Fischer, et al.
Genomics|May 1, 1992
Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersS Somlo, B Wirth, G G Germino, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellitesB Wirth, A el-Agwany, A Baasner, et al.
Archives of Dermatological Research|January 1, 1989
Gene diagnosis in X-linked ichthyosisF H Herrmann, B Wirth, K Wulff, et al.
Nature Genetics|September 10, 1998
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomicsJ M Scharf, M G Endrizzi, A Wetter, et al.
Revue Neurologique|July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathiesC Paketci, M Karakaya, P Edem, et al.
American Journal of Human Genetics|December 1, 1994
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophyC J DiDonato, K Morgan, J D Carpten, et al.
Pageof 12

Showing results (101-110 of 119) with videos related to

Sort By:
Pageof 12
Human Genetics|November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelicB Wirth, K Zerres, M Fischbach, et al.
Orphanet Journal of Rare Diseases|May 3, 2023
Objective measurement of oral function in adults with spinal muscular atrophyT Kruse, S Shamai, D Leflerovà, et al.
Human Genetics|October 1, 1988
Linkage analysis in X-linked ichthyosis (steroid sulfatase deficiency)B Wirth, F H Herrmann, M Neugebauer, et al.
American Journal of Nephrology|January 1, 1988
Late manifestation of autosomal-recessive polycystic kidney disease in two sistersH P Neumann, K Zerres, C L Fischer, et al.
Genomics|May 1, 1992
Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersS Somlo, B Wirth, G G Germino, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellitesB Wirth, A el-Agwany, A Baasner, et al.
Archives of Dermatological Research|January 1, 1989
Gene diagnosis in X-linked ichthyosisF H Herrmann, B Wirth, K Wulff, et al.
Nature Genetics|September 10, 1998
Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomicsJ M Scharf, M G Endrizzi, A Wetter, et al.
Revue Neurologique|July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathiesC Paketci, M Karakaya, P Edem, et al.
American Journal of Human Genetics|December 1, 1994
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophyC J DiDonato, K Morgan, J D Carpten, et al.
Pageof 12