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K-H Grzeschik

Showing results (61-70 of 162) with videos related to

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Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1988
Evaluation of random cDNA clones as probes for human restriction fragment length polymorphismsC Wappenschmidt, M Higuchi, C Meisen, et al.
The EMBO Journal|August 1, 1984
Actin-like sequences are present on human X and Y chromosomesR Heilig, A Hanauer, K H Grzeschik, et al.
Genomics|March 15, 1997
The human hepatocyte nuclear factor 3/fork head gene FKHL13: genomic structure and pattern of expressionD B Murphy, S Seemann, S Wiese, et al.
American Journal of Human Genetics|May 1, 1990
The gene for the alpha polypeptide of pyruvate dehydrogenase is X-linked in humansP Szabo, K F Sheu, R M Robinson, et al.
Genomics|June 1, 1993
All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6W Albig, B Drabent, J Kunz, et al.
Human Genetics|October 1, 1991
The human transmembrane secretory component (poly-Ig receptor): molecular cloning, restriction fragment length polymorphism and chromosomal sublocalizationP Krajci, K H Grzeschik, A H Geurts van Kessel, et al.
Somatic Cell and Molecular Genetics|May 1, 1988
Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybridsW J Rettig, K H Grzeschik, A K Yenamandra, et al.
Genomics|August 1, 1994
Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene regionA Vortkamp, M Gessler, D Le Paslier, et al.
Human Genetics|September 1, 1989
Regional localization of human ecto-5' nucleotidase to chromosome 6q14-q21J M Boyle, Y Hey, K H Grzeschik, et al.
Human Molecular Genetics|September 25, 1997
Point mutations in human GLI3 cause Greig syndromeA Wild, M Kalff-Suske, A Vortkamp, et al.
Pageof 17

Showing results (61-70 of 162) with videos related to

Sort By:
Pageof 17
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1988
Evaluation of random cDNA clones as probes for human restriction fragment length polymorphismsC Wappenschmidt, M Higuchi, C Meisen, et al.
The EMBO Journal|August 1, 1984
Actin-like sequences are present on human X and Y chromosomesR Heilig, A Hanauer, K H Grzeschik, et al.
Genomics|March 15, 1997
The human hepatocyte nuclear factor 3/fork head gene FKHL13: genomic structure and pattern of expressionD B Murphy, S Seemann, S Wiese, et al.
American Journal of Human Genetics|May 1, 1990
The gene for the alpha polypeptide of pyruvate dehydrogenase is X-linked in humansP Szabo, K F Sheu, R M Robinson, et al.
Genomics|June 1, 1993
All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6W Albig, B Drabent, J Kunz, et al.
Human Genetics|October 1, 1991
The human transmembrane secretory component (poly-Ig receptor): molecular cloning, restriction fragment length polymorphism and chromosomal sublocalizationP Krajci, K H Grzeschik, A H Geurts van Kessel, et al.
Somatic Cell and Molecular Genetics|May 1, 1988
Definition of selectable cell surface markers for human chromosomes and chromosome segments in rodent-human hybridsW J Rettig, K H Grzeschik, A K Yenamandra, et al.
Genomics|August 1, 1994
Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene regionA Vortkamp, M Gessler, D Le Paslier, et al.
Human Genetics|September 1, 1989
Regional localization of human ecto-5' nucleotidase to chromosome 6q14-q21J M Boyle, Y Hey, K H Grzeschik, et al.
Human Molecular Genetics|September 25, 1997
Point mutations in human GLI3 cause Greig syndromeA Wild, M Kalff-Suske, A Vortkamp, et al.
Pageof 17