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M Mächler

Showing results (1-10 of 18) with videos related to

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Neurofibromatosis|January 1, 1989
Neurofibromatosis type 1 in a child of a parent with segmental neurofibromatosis (NF-5)E Boltshauser, H Stocker, M Mächler
Schweizerische Medizinische Wochenschrift|December 19, 1987
[DNA diagnosis of Huntington's chorea. Application and genetic counseling in 4 involved families]J Hammer, M Mächler, W Schmid
Forensic Science International|October 1, 1988
Postmortem stability of DNAW Bär, A Kratzer, M Mächler, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1990
[X-chromosomal hereditary night blindness: detection of carriers by segregation analysis with linked DNA markers]U Orth, A Schinzel, M Mächler, et al.
Nucleic Acids Research|December 10, 1983
A functional component of the sea urchin H2A gene modulator contains an extended sequence homology to a viral enhancerR Grosschedl, M Mächler, U Rohrer, et al.
Lancet (London, England)|November 7, 1987
Linked DNA markers in clinical diagnosis of juvenile Huntington's diseaseJ Hammer, M Mächler, W Schmid, et al.
Nucleic Acids Research|August 25, 1990
A second NsiI RFLP at the CYBB locusT J Mühlebach, W Robinson, R A Seger, et al.
Cell|May 1, 1979
Sequence organization of the spacer DNA in a ribosomal gene unit of Xenopus laevisP Boseley, T Moss, M Mächler, et al.
Human Heredity|January 1, 1990
Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblingsJ Ott, J Caesar, M Mächler, et al.
Schweizerische Medizinische Wochenschrift|October 5, 1991
[Neurofibromatosis Type 1: genetic studies with DNA markers in 38 families]R Spiegel, M Mächler, H P Stocker, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Neurofibromatosis|January 1, 1989
Neurofibromatosis type 1 in a child of a parent with segmental neurofibromatosis (NF-5)E Boltshauser, H Stocker, M Mächler
Schweizerische Medizinische Wochenschrift|December 19, 1987
[DNA diagnosis of Huntington's chorea. Application and genetic counseling in 4 involved families]J Hammer, M Mächler, W Schmid
Forensic Science International|October 1, 1988
Postmortem stability of DNAW Bär, A Kratzer, M Mächler, et al.
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1990
[X-chromosomal hereditary night blindness: detection of carriers by segregation analysis with linked DNA markers]U Orth, A Schinzel, M Mächler, et al.
Nucleic Acids Research|December 10, 1983
A functional component of the sea urchin H2A gene modulator contains an extended sequence homology to a viral enhancerR Grosschedl, M Mächler, U Rohrer, et al.
Lancet (London, England)|November 7, 1987
Linked DNA markers in clinical diagnosis of juvenile Huntington's diseaseJ Hammer, M Mächler, W Schmid, et al.
Nucleic Acids Research|August 25, 1990
A second NsiI RFLP at the CYBB locusT J Mühlebach, W Robinson, R A Seger, et al.
Cell|May 1, 1979
Sequence organization of the spacer DNA in a ribosomal gene unit of Xenopus laevisP Boseley, T Moss, M Mächler, et al.
Human Heredity|January 1, 1990
Presymptomatic exclusion of myotonic dystrophy in a one-generation pedigree of half-siblingsJ Ott, J Caesar, M Mächler, et al.
Schweizerische Medizinische Wochenschrift|October 5, 1991
[Neurofibromatosis Type 1: genetic studies with DNA markers in 38 families]R Spiegel, M Mächler, H P Stocker, et al.
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