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B Zoll

Showing results (11-20 of 63) with videos related to

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Clinical Genetics|February 1, 1993
A case of full triploidy (69,XXX) of paternal origin with unusually long survival timeS C Niemann-Seyde, H Rehder, B Zoll
Prenatal Diagnosis|May 1, 1990
Prenatal diagnosis and postnatal follow-up of a child with two de novo unrelated balanced reciprocal translocationsM Pruggmayer, B Zoll, M Leipoldt, et al.
Blut|January 1, 1990
Diagnosis of haemophilia B using the polymerase chain reactionJ Reiss, U Neufeldt, K Wieland, et al.
Journal of Neurology|July 1, 1991
Amplification of the c-erbB oncogene is associated with malignancy in primary tumours of neuroepithelial tissueU Diedrich, S Soja, J Behnke, et al.
The British Journal of Dermatology|June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?S Schauder, F Hanefeld, U M Noske, et al.
Clinical Genetics|October 1, 1991
Saethre-Chotzen syndrome (ACS III) in four generationsS C Niemann-Seyde, S W Eber, B Zoll
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Fetal alcohol syndrome in association with Rett syndromeB Zoll, P Huppke, A Wessel, et al.
Der Nervenarzt|October 1, 1991
[Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers]U Thies, K Schröder, B Bockel, et al.
Human Genetics|June 1, 1994
Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg familiesC Meyer-Kleine, M Otto, B Zoll, et al.
American Journal of Medical Genetics|December 1, 1989
Down syndrome at birth not detected by first-trimester chorionic villus samplingI Bartels, I Hansmann, U Holland, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Clinical Genetics|February 1, 1993
A case of full triploidy (69,XXX) of paternal origin with unusually long survival timeS C Niemann-Seyde, H Rehder, B Zoll
Prenatal Diagnosis|May 1, 1990
Prenatal diagnosis and postnatal follow-up of a child with two de novo unrelated balanced reciprocal translocationsM Pruggmayer, B Zoll, M Leipoldt, et al.
Blut|January 1, 1990
Diagnosis of haemophilia B using the polymerase chain reactionJ Reiss, U Neufeldt, K Wieland, et al.
Journal of Neurology|July 1, 1991
Amplification of the c-erbB oncogene is associated with malignancy in primary tumours of neuroepithelial tissueU Diedrich, S Soja, J Behnke, et al.
The British Journal of Dermatology|June 10, 2000
Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?S Schauder, F Hanefeld, U M Noske, et al.
Clinical Genetics|October 1, 1991
Saethre-Chotzen syndrome (ACS III) in four generationsS C Niemann-Seyde, S W Eber, B Zoll
Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Fetal alcohol syndrome in association with Rett syndromeB Zoll, P Huppke, A Wessel, et al.
Der Nervenarzt|October 1, 1991
[Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers]U Thies, K Schröder, B Bockel, et al.
Human Genetics|June 1, 1994
Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg familiesC Meyer-Kleine, M Otto, B Zoll, et al.
American Journal of Medical Genetics|December 1, 1989
Down syndrome at birth not detected by first-trimester chorionic villus samplingI Bartels, I Hansmann, U Holland, et al.
Pageof 7