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K Zerres

Showing results (91-100 of 174) with videos related to

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European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1988
Prenatal diagnosis and management in fetuses with cystic hygromata colliU Gembruch, M Hansmann, R Bald, et al.
European Journal of Pediatrics|September 4, 1998
Clinical features of unilateral multicystic renal dysplasia in childrenS Rudnik-Schöneborn, U John, F Deget, et al.
European Journal of Pediatrics|June 23, 1999
Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counsellingF Haverkamp, J Wölfle, M Aretz, et al.
Journal of the Neurological Sciences|February 27, 1997
A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 patientsK Zerres, S Rudnik-Schöneborn, E Forrest, et al.
Kidney International|November 1, 1990
Congenital hepatic fibrosis in autosomal-dominant polycystic kidney diseaseJ M Cobben, M H Breuning, C Schoots, et al.
Molecular Syndromology|December 23, 2011
Two Adult Patients with Ellis-van Creveld Syndrome Extending the Clinical SpectrumS Rudnik-Schöneborn, K Zerres, L Graul-Neumann, et al.
Klinische Padiatrie|July 1, 1987
[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis]G Schmid, F Haverkamp, J Rechmann, et al.
Neuropediatrics|December 19, 2009
Andermann syndrome can be a phenocopy of hereditary motor and sensory neuropathy--report of a discordant sibship with a compound heterozygous mutation of the KCC3 geneS Rudnik-Schöneborn, U Hehr, T von Kalle, et al.
Alcohol and Alcoholism (Oxford, Oxfordshire)|April 4, 2015
Alcohol Consumption in Healthy OPRM1 G Allele Carriers and Its Association with Impulsive BehaviorP Pfeifer, M Sariyar, T Eggermann, et al.
European Neurology|May 30, 1998
Analysis of creatine kinase activity in 504 patients with proximal spinal muscular atrophy types I-III from the point of view of progression and severityS Rudnik-Schöneborn, S Lützenrath, J Borkowska, et al.
Pageof 18

Showing results (91-100 of 174) with videos related to

Sort By:
Pageof 18
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1988
Prenatal diagnosis and management in fetuses with cystic hygromata colliU Gembruch, M Hansmann, R Bald, et al.
European Journal of Pediatrics|September 4, 1998
Clinical features of unilateral multicystic renal dysplasia in childrenS Rudnik-Schöneborn, U John, F Deget, et al.
European Journal of Pediatrics|June 23, 1999
Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counsellingF Haverkamp, J Wölfle, M Aretz, et al.
Journal of the Neurological Sciences|February 27, 1997
A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 patientsK Zerres, S Rudnik-Schöneborn, E Forrest, et al.
Kidney International|November 1, 1990
Congenital hepatic fibrosis in autosomal-dominant polycystic kidney diseaseJ M Cobben, M H Breuning, C Schoots, et al.
Molecular Syndromology|December 23, 2011
Two Adult Patients with Ellis-van Creveld Syndrome Extending the Clinical SpectrumS Rudnik-Schöneborn, K Zerres, L Graul-Neumann, et al.
Klinische Padiatrie|July 1, 1987
[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis]G Schmid, F Haverkamp, J Rechmann, et al.
Neuropediatrics|December 19, 2009
Andermann syndrome can be a phenocopy of hereditary motor and sensory neuropathy--report of a discordant sibship with a compound heterozygous mutation of the KCC3 geneS Rudnik-Schöneborn, U Hehr, T von Kalle, et al.
Alcohol and Alcoholism (Oxford, Oxfordshire)|April 4, 2015
Alcohol Consumption in Healthy OPRM1 G Allele Carriers and Its Association with Impulsive BehaviorP Pfeifer, M Sariyar, T Eggermann, et al.
European Neurology|May 30, 1998
Analysis of creatine kinase activity in 504 patients with proximal spinal muscular atrophy types I-III from the point of view of progression and severityS Rudnik-Schöneborn, S Lützenrath, J Borkowska, et al.
Pageof 18