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J Murken

Showing results (11-20 of 33) with videos related to

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Human Genetics|August 21, 2001
AcroM fluorescent in situ hybridization analyses of marker chromosomesS Langer, C Fauth, M Rocchi, et al.
Human Genetics|July 1, 1990
Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogeneticsA Jauch, C Daumer, P Lichter, et al.
Clinical Genetics|November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boyS Schuffenhauer, D F Callen, H Seidel, et al.
Journal of Medical Genetics|April 16, 1999
De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findingsS Schuffenhauer, H J Leifheit, P Lichtner, et al.
American Journal of Medical Genetics|May 8, 1999
No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585O Bartsch, A Wagner, G K Hinkel, et al.
Journal of Medical Genetics|February 24, 2001
Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetryH Schmidt, S Uhrig, G Lederer, et al.
Der Internist|June 4, 1999
[29-year-old patient with gynecomastia and small testis]S Brand, T M Strom, M M Weber, et al.
Der Nervenarzt|October 1, 1991
[Neurogenetics--the challenge for neurology. 1. Neurogenetic diseases]T Gasser, C Trenkwalder, T Meitinger, et al.
Annales De Genetique|January 1, 1995
DiGeorge syndrome and partial monosomy 10p: case report and reviewS Schuffenhauer, H Seidel, H Oechsler, et al.
Nature Genetics|December 1, 1993
Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structureT Meitinger, A Meindl, P Bork, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Human Genetics|August 21, 2001
AcroM fluorescent in situ hybridization analyses of marker chromosomesS Langer, C Fauth, M Rocchi, et al.
Human Genetics|July 1, 1990
Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogeneticsA Jauch, C Daumer, P Lichter, et al.
Clinical Genetics|November 1, 1992
De novo interstitial deletion 16(q12.1q13) of paternal origin in a 10-year-old boyS Schuffenhauer, D F Callen, H Seidel, et al.
Journal of Medical Genetics|April 16, 1999
De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findingsS Schuffenhauer, H J Leifheit, P Lichtner, et al.
American Journal of Medical Genetics|May 8, 1999
No evidence for chromosomal microdeletions at the second DiGeorge syndrome locus on 10p near D10S585O Bartsch, A Wagner, G K Hinkel, et al.
Journal of Medical Genetics|February 24, 2001
Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetryH Schmidt, S Uhrig, G Lederer, et al.
Der Internist|June 4, 1999
[29-year-old patient with gynecomastia and small testis]S Brand, T M Strom, M M Weber, et al.
Der Nervenarzt|October 1, 1991
[Neurogenetics--the challenge for neurology. 1. Neurogenetic diseases]T Gasser, C Trenkwalder, T Meitinger, et al.
Annales De Genetique|January 1, 1995
DiGeorge syndrome and partial monosomy 10p: case report and reviewS Schuffenhauer, H Seidel, H Oechsler, et al.
Nature Genetics|December 1, 1993
Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structureT Meitinger, A Meindl, P Bork, et al.
Pageof 4