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Human Genetics
|
November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelic
B 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 atrophy
T 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 sisters
H 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 markers
S 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 microsatellites
B Wirth, A el-Agwany, A Baasner, et al.
Archives of Dermatological Research
|
January 1, 1989
Gene diagnosis in X-linked ichthyosis
F 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 genomics
J M Scharf, M G Endrizzi, A Wetter, et al.
Revue Neurologique
|
July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies
C 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 atrophy
C J DiDonato, K Morgan, J D Carpten, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 119) with videos related to
Sort By:
Page
of 12
Human Genetics
|
November 1, 1987
Autosomal recessive and dominant forms of polycystic kidney disease are not allelic
B 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 atrophy
T 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 sisters
H 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 markers
S 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 microsatellites
B Wirth, A el-Agwany, A Baasner, et al.
Archives of Dermatological Research
|
January 1, 1989
Gene diagnosis in X-linked ichthyosis
F 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 genomics
J M Scharf, M G Endrizzi, A Wetter, et al.
Revue Neurologique
|
July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies
C 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 atrophy
C J DiDonato, K Morgan, J D Carpten, et al.
Page
of 12