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S Schuffenhauer

Showing results (21-30 of 45) with videos related to

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Human Genetics|July 8, 1998
Deletion mapping by FISH with BACs in patients with partial monosomy 22q13K Schröder, S Schuffenhauer, H Seidel, et al.
American Journal of Medical Genetics|December 1, 1994
Tetrasomy 21 pter-->q22.1 and Down syndrome: molecular definition of the regionC Daumer-Haas, S Schuffenhauer, J U Walther, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10pP Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
Human Genetics|June 1, 1996
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)M Erdel, S Schuffenhauer, B Buchholz, et al.
American Journal of Medical Genetics|May 3, 1996
Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7pS von Gernet, S Schuffenhauer, A Golla, et al.
Human Genetics|March 1, 1997
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 regionJ Deckert, M M Nöthen, S P Bryant, et al.
American Journal of Human Genetics|April 14, 2000
An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISHJ Azofeifa, C Fauth, J Kraus, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Increased parental ages and uniparental disomy 15: a paternal age effect?W P Robinson, I Lorda-Sanchez, S Malcolm, et al.
Pigment Cell Research|December 1, 1994
The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2M H Brilliant, R King, U Francke, et al.
Clinical Genetics|August 1, 1996
Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the motherC Apacik, M Cohen, M Jakobeit, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Human Genetics|July 8, 1998
Deletion mapping by FISH with BACs in patients with partial monosomy 22q13K Schröder, S Schuffenhauer, H Seidel, et al.
American Journal of Medical Genetics|December 1, 1994
Tetrasomy 21 pter-->q22.1 and Down syndrome: molecular definition of the regionC Daumer-Haas, S Schuffenhauer, J U Walther, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Expression and mutation analysis of BRUNOL3, a candidate gene for heart and thymus developmental defects associated with partial monosomy 10pP Lichtner, T Attié-Bitach, S Schuffenhauer, et al.
Human Genetics|June 1, 1996
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)M Erdel, S Schuffenhauer, B Buchholz, et al.
American Journal of Medical Genetics|May 3, 1996
Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7pS von Gernet, S Schuffenhauer, A Golla, et al.
Human Genetics|March 1, 1997
Mapping of the human adenosine A2a receptor gene: relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 regionJ Deckert, M M Nöthen, S P Bryant, et al.
American Journal of Human Genetics|April 14, 2000
An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISHJ Azofeifa, C Fauth, J Kraus, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Increased parental ages and uniparental disomy 15: a paternal age effect?W P Robinson, I Lorda-Sanchez, S Malcolm, et al.
Pigment Cell Research|December 1, 1994
The mouse pink-eyed dilution gene: association with hypopigmentation in Prader-Willi and Angelman syndromes and with human OCA2M H Brilliant, R King, U Francke, et al.
Clinical Genetics|August 1, 1996
Two brothers with multiple congenital anomalies and mental retardation due to disomy (X)(q12-->q13.3) inherited from the motherC Apacik, M Cohen, M Jakobeit, et al.
Pageof 5