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Showing results (71-80 of 174) with videos related to

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Klinische Padiatrie|September 14, 2011
Long term peritoneal dialysis in an anuric preterm infant - a futile treatment?D Faas, D Klauwer, G Klaus, et al.
Annales De Genetique|January 1, 1990
Prenatal detection of heart defects as an indication for chromosome analysisG Schwanitz, K Zerres, U Gembruch, et al.
European Journal of Clinical Investigation|February 18, 2003
Vitamin D receptor gene polymorphism BsmI is not associated with the prevalence and severity of CAD in a large-scale angiographic cohort of 3441 patientsJ R Ortlepp, A von Korff, P Hanrath, et al.
The Turkish Journal of Pediatrics|July 25, 1998
Autosomal recessive polycystic kidney disease: mapping to chromosomal region of 6p21-cen in a Turkish childN Beşbaş, S Ozen, U Saatçi, et al.
American Journal of Medical Genetics|December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndromeP Rabe, F Haverkamp, D Emons, et al.
Annales De Genetique|January 1, 1996
Further arguments for non-fortuitous association of Potter sequence with XYY malesS Rudnik-Schöneborn, H M Schüler, G Schwanitz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 18, 1999
Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney diseaseH P Neumann, B Krumme, V van Velthoven, et al.
American Journal of Medical Genetics|October 1, 1991
MASA syndrome: clinical variability and linkage analysisM Rietschel, W Friedl, S Uhlhaas, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[An at-risk pregnancy of a carrier of cystic fibrosis (mucoviscidosis) with a new partner]J Reiss, M Krawczak, A Gal, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
[Non-directivity as a guiding category in human genetic counselling in a historical perspective]F Söhner, V Rolfes, W Hofmann, et al.
Pageof 18

Showing results (71-80 of 174) with videos related to

Sort By:
Pageof 18
Klinische Padiatrie|September 14, 2011
Long term peritoneal dialysis in an anuric preterm infant - a futile treatment?D Faas, D Klauwer, G Klaus, et al.
Annales De Genetique|January 1, 1990
Prenatal detection of heart defects as an indication for chromosome analysisG Schwanitz, K Zerres, U Gembruch, et al.
European Journal of Clinical Investigation|February 18, 2003
Vitamin D receptor gene polymorphism BsmI is not associated with the prevalence and severity of CAD in a large-scale angiographic cohort of 3441 patientsJ R Ortlepp, A von Korff, P Hanrath, et al.
The Turkish Journal of Pediatrics|July 25, 1998
Autosomal recessive polycystic kidney disease: mapping to chromosomal region of 6p21-cen in a Turkish childN Beşbaş, S Ozen, U Saatçi, et al.
American Journal of Medical Genetics|December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndromeP Rabe, F Haverkamp, D Emons, et al.
Annales De Genetique|January 1, 1996
Further arguments for non-fortuitous association of Potter sequence with XYY malesS Rudnik-Schöneborn, H M Schüler, G Schwanitz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 18, 1999
Multiple intracranial aneurysms in a patient with autosomal recessive polycystic kidney diseaseH P Neumann, B Krumme, V van Velthoven, et al.
American Journal of Medical Genetics|October 1, 1991
MASA syndrome: clinical variability and linkage analysisM Rietschel, W Friedl, S Uhlhaas, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1989
[An at-risk pregnancy of a carrier of cystic fibrosis (mucoviscidosis) with a new partner]J Reiss, M Krawczak, A Gal, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
[Non-directivity as a guiding category in human genetic counselling in a historical perspective]F Söhner, V Rolfes, W Hofmann, et al.
Pageof 18