Suchergebnisse - "Cremer, Marion"

PubPharm (13)

1

SOFTWARE AND BOOK REVIEWS - Quality Food in Quantity: Management and Science

enthalten in: Journal of restaurant & foodservice marketing | 1999

von Parsa, H. | Cremer, M. | Parsa, H.

2

High-resolution comparative hybridization to combed DNA fibers

enthalten in: Human genetics | 1997

von Kraus, J. | Weber, R. | Cremer, M. | +7

3

Myotonic Dystrophy: The Role of Large Triplet Repeat Length in the Development of Mental Retardation

enthalten in: Archives of neurology | 1997

von Spranger, M. | Spranger, S. | Tischendorf, M. | +2

4

Lack of a BglII site at the 5′ region of the PGK 1 locus: a new variant discovered in two Chibchan Amerindian groups from Costa Rica

enthalten in: Human genetics | 1995

von Azofeifa, J. | Barrantes, R. | Cremer, M.

5

X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes

enthalten in: Human genetics | 1995

von Azofeifa, J. | Voit, T. | Hübner, C. | +1

6

Fluoreszenz-in-situ-Hybridisierung (FISH)

enthalten in: Deutsches Ärzteblatt | 1995

von Cremer, T. | Jauch, A. | Ried, T. | +4

7

Multicolor fluorescence in situ hybridization on metaphase chromosomes and interphase Halo-preparations using cosmid and YAC clones for the simultaneous high resolution mapping of deletions in the dystrophin gene

enthalten in: Human genetics | 1994

von Tocharoentanaphol, C. | Cremer, M. | Schröck, E. | +4

8

Rapid Publication: Gene for Simpson-Golabi-Behmel Syndrome Is Linked to HPRT in Xq26 in Two European Families

enthalten in: American journal of medical genetics | 1994

von Orth, U. | Gurrieri, F. | Behmel, A. | +4

9

Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8

enthalten in: Human genetics | 1989

von Mao, Y. | Cremer, M.

10

Quantitative and qualitative assay of amniotic-fluid acetylcholinesterase in the prenatal diagnosis of neural tube defects

enthalten in: Human genetics | 1981

von Voigtländer, T. | Friedl, W. | Cremer, M. | +2