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O Bartsch

Showing results (11-20 of 65) with videos related to

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Neuropediatrics|December 1, 1992
Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspectsU Thyen, F Aksu, O Bartsch, et al.
Cytogenetics and Cell Genetics|August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial caseO Bartsch, W Kress, A Wagner, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1992
[Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes]O Bartsch, F Aksu, A Fenner, et al.
Laryngo- Rhino- Otologie|November 8, 2014
[Congenital sensorineural deafness with microtia and Michel aplasia]A K Läßig, O Bartsch, U Zechner, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Unexpected death of a 12 year old boy with monosomy 1p36L M Neumann, T Polster, T Spantzel, et al.
Journal of Medical Genetics|March 2, 1999
Severe complications and gastric carcinoma in Mulvihill-Smith syndromeO Bartsch, D Ludwig, E Schwinger, et al.
Genetic Counseling (Geneva, Switzerland)|August 5, 2009
A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24)S Balci, E Aypar, M S Beksaç, et al.
Klinische Monatsblatter Fur Augenheilkunde|June 1, 1992
[Bilateral colobomatous microphthalmus with orbital giant cysts in incomplete tetrasomy 22]W Lange, R Rochels, J Otte, et al.
HNO|September 5, 2003
[DiGeorge syndrome/velcardiofacial syndrome: oral and maxillofacial surgery]W Pradel, O Bartsch, R Müller, et al.
Journal of Medical Genetics|September 1, 1994
Mulvihill-Smith syndrome: case report and reviewO Bartsch, K D Tympner, E Schwinger, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
Neuropediatrics|December 1, 1992
Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspectsU Thyen, F Aksu, O Bartsch, et al.
Cytogenetics and Cell Genetics|August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial caseO Bartsch, W Kress, A Wagner, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 1, 1992
[Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes]O Bartsch, F Aksu, A Fenner, et al.
Laryngo- Rhino- Otologie|November 8, 2014
[Congenital sensorineural deafness with microtia and Michel aplasia]A K Läßig, O Bartsch, U Zechner, et al.
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Unexpected death of a 12 year old boy with monosomy 1p36L M Neumann, T Polster, T Spantzel, et al.
Journal of Medical Genetics|March 2, 1999
Severe complications and gastric carcinoma in Mulvihill-Smith syndromeO Bartsch, D Ludwig, E Schwinger, et al.
Genetic Counseling (Geneva, Switzerland)|August 5, 2009
A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24)S Balci, E Aypar, M S Beksaç, et al.
Klinische Monatsblatter Fur Augenheilkunde|June 1, 1992
[Bilateral colobomatous microphthalmus with orbital giant cysts in incomplete tetrasomy 22]W Lange, R Rochels, J Otte, et al.
HNO|September 5, 2003
[DiGeorge syndrome/velcardiofacial syndrome: oral and maxillofacial surgery]W Pradel, O Bartsch, R Müller, et al.
Journal of Medical Genetics|September 1, 1994
Mulvihill-Smith syndrome: case report and reviewO Bartsch, K D Tympner, E Schwinger, et al.
Pageof 7