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K Zerres

Showing results (21-30 of 174) with videos related to

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Clinical Nephrology|October 13, 2001
DNA diagnosis in hereditary nephropathiesK Zerres, T Eggermann, S Rudnik-Schöneborn
Neuromuscular Disorders : NMD|May 1, 1997
Spinal muscular atrophy--clinical and genetic correlationsK Zerres, B Wirth, S Rudnik-Schöneborn
Human Genetics|June 1, 1994
Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4K Zerres, G Mücher, S Rudnik-Schöneborn
Human Genetics|January 1, 1984
Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosisK Zerres, M C Völpel, H Weiss
American Journal of Human Genetics|July 1, 1994
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophyS Rudnik-Schöneborn, B Wirth, K Zerres
Geburtshilfe Und Frauenheilkunde|May 1, 1990
[Pregnancy in Crohn disease and ulcerative colitis. Maternal and fetal risks]F Haverkamp, D Normann, W Küster, et al.
Annales De Genetique|January 1, 1993
Chromosomal findings in fetuses with ultrasonographically diagnosed ventriculomegalyG Schwanitz, H Schüler, U Gembruch, et al.
Klinische Padiatrie|April 17, 2012
Stress and coping in parents of children and adolescents with spinal muscular atrophyA von Gontard, S Rudnik-Schöneborn, K Zerres
Journal of Inherited Metabolic Disease|January 26, 2006
Search for mutations in SLC1A5 (19q13) in cystinuria patientsE Brauers, U Vester, K Zerres, et al.
Clinical Nephrology|April 25, 2006
Functional characterization of SLC7A9 polymorphisms assumed to influence the cystinuria phenotypeE Brauers, C Schmidt, K Zerres, et al.
Pageof 18

Showing results (21-30 of 174) with videos related to

Sort By:
Pageof 18
Clinical Nephrology|October 13, 2001
DNA diagnosis in hereditary nephropathiesK Zerres, T Eggermann, S Rudnik-Schöneborn
Neuromuscular Disorders : NMD|May 1, 1997
Spinal muscular atrophy--clinical and genetic correlationsK Zerres, B Wirth, S Rudnik-Schöneborn
Human Genetics|June 1, 1994
Autosomal recessive polycystic kidney disease does not map to the second gene locus for autosomal dominant polycystic kidney disease on chromosome 4K Zerres, G Mücher, S Rudnik-Schöneborn
Human Genetics|January 1, 1984
Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosisK Zerres, M C Völpel, H Weiss
American Journal of Human Genetics|July 1, 1994
Evidence of autosomal dominant mutations in childhood-onset proximal spinal muscular atrophyS Rudnik-Schöneborn, B Wirth, K Zerres
Geburtshilfe Und Frauenheilkunde|May 1, 1990
[Pregnancy in Crohn disease and ulcerative colitis. Maternal and fetal risks]F Haverkamp, D Normann, W Küster, et al.
Annales De Genetique|January 1, 1993
Chromosomal findings in fetuses with ultrasonographically diagnosed ventriculomegalyG Schwanitz, H Schüler, U Gembruch, et al.
Klinische Padiatrie|April 17, 2012
Stress and coping in parents of children and adolescents with spinal muscular atrophyA von Gontard, S Rudnik-Schöneborn, K Zerres
Journal of Inherited Metabolic Disease|January 26, 2006
Search for mutations in SLC1A5 (19q13) in cystinuria patientsE Brauers, U Vester, K Zerres, et al.
Clinical Nephrology|April 25, 2006
Functional characterization of SLC7A9 polymorphisms assumed to influence the cystinuria phenotypeE Brauers, C Schmidt, K Zerres, et al.
Pageof 18