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K Zerres

Showing results (51-60 of 174) with videos related to

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Klinische Padiatrie|November 1, 1990
[7-week-old infant with a hydrolethalus syndrome: case report, differential diagnosis and literature review]F Haverkamp, K Zerres, H Fahnenstich, et al.
Annales De Genetique|January 1, 1989
Duplication 7p de novo and literature reviewK Zerres, G Schwanitz, K Gellissen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 30, 2001
Neurodevelopmental risks in twin-to-twin transfusion syndrome: preliminary findingsF Haverkamp, C Lex, C Hanisch, et al.
Geburtshilfe Und Frauenheilkunde|August 1, 1984
[Prenatal diagnosis of thanatophoric dwarfism with a cloverleaf skull--ultrasonographic findings, humane genetic aspects]H Weiss, U Rosseck, K Zerres, et al.
Annales De Genetique|January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17G Schwanitz, K Zerres, M Niesen, et al.
International Journal of Pediatric Otorhinolaryngology|January 1, 1996
Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstructionF Haverkamp, D Emons, H J Straehler-Pohl, et al.
American Journal of Medical Genetics|May 15, 1994
Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implicationsS Rudnik-Schöneborn, D Röhrig, G Morgan, et al.
Journal of Medical Genetics|March 1, 1995
Familial schizencephaly: further delineation of a rare disorderF Haverkamp, K Zerres, B Ostertun, et al.
Neuromuscular Disorders : NMD|August 8, 2008
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotypeS Rudnik-Schöneborn, J Weis, W Kress, et al.
Neuroscience Letters|October 21, 1998
Apolipoprotein E polymorphism influences the cerebral metabolic pattern in Alzheimer's diseaseR Mielke, K Zerres, S Uhlhaas, et al.
Pageof 18

Showing results (51-60 of 174) with videos related to

Sort By:
Pageof 18
Klinische Padiatrie|November 1, 1990
[7-week-old infant with a hydrolethalus syndrome: case report, differential diagnosis and literature review]F Haverkamp, K Zerres, H Fahnenstich, et al.
Annales De Genetique|January 1, 1989
Duplication 7p de novo and literature reviewK Zerres, G Schwanitz, K Gellissen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 30, 2001
Neurodevelopmental risks in twin-to-twin transfusion syndrome: preliminary findingsF Haverkamp, C Lex, C Hanisch, et al.
Geburtshilfe Und Frauenheilkunde|August 1, 1984
[Prenatal diagnosis of thanatophoric dwarfism with a cloverleaf skull--ultrasonographic findings, humane genetic aspects]H Weiss, U Rosseck, K Zerres, et al.
Annales De Genetique|January 1, 1988
Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17G Schwanitz, K Zerres, M Niesen, et al.
International Journal of Pediatric Otorhinolaryngology|January 1, 1996
Craniometaphyseal dysplasia as a rare cause of a severe neonatal nasal obstructionF Haverkamp, D Emons, H J Straehler-Pohl, et al.
American Journal of Medical Genetics|May 15, 1994
Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implicationsS Rudnik-Schöneborn, D Röhrig, G Morgan, et al.
Journal of Medical Genetics|March 1, 1995
Familial schizencephaly: further delineation of a rare disorderF Haverkamp, K Zerres, B Ostertun, et al.
Neuromuscular Disorders : NMD|August 8, 2008
Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotypeS Rudnik-Schöneborn, J Weis, W Kress, et al.
Neuroscience Letters|October 21, 1998
Apolipoprotein E polymorphism influences the cerebral metabolic pattern in Alzheimer's diseaseR Mielke, K Zerres, S Uhlhaas, et al.
Pageof 18