Resultats de la cerca - M.E. Kalf
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1
Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase per Saskia A.J. Lesnik Oberstein, Marjolein Kriek, Stefan J. White, M.E. Kalf, Károly Szuhai, Johan T. den Dunnen, Martijn H. Breuning, Raoul C. M. Hennekam
Publicat 2006Artigo -
2
Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization per Stefan J. White, M.E. Kalf, Qiang Liu, Michel P Villerius, Dieuwke Engelsma, Marjolein Kriek, Ellen Vollebregt, Egbert Bakker, Gert‐Jan B. van Ommen, Martijn H. Breuning, Johan T. den Dunnen
Publicat 2002Artigo -
3
Successful Long-Term Growth Hormone Therapy in a Girl with Haploinsufficiency of the Insulin-Like Growth Factor-I Receptor due to a Terminal 15q26.2->qter Deletion Detected... per M.J.E. Walenkamp, Sabine M.P.F. de Muinck Keizer‐Schrama, Marianne de Mos, M.E. Kalf, Hermine A. van Duyvenvoorde, Annemieke M. Boot, Sarina G. Kant, Stefan J. White, Monique Losekoot, Johan T. den Dunnen, Marcel Karperien, Jan M. Wit
Publicat 2008Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Comparative genomic hybridization
Endocrinology
Exon
Genome
Molecular biology
Multiplex ligation-dependent probe amplification
Mutation
Short stature
Chromosome
Computational biology
Copy-number variation
Duchenne muscular dystrophy
Gene dosage
Gene duplication
Gene expression
Glycosyltransferase
Growth factor
Haploinsufficiency
Insulin-like growth factor 1 receptor
Internal medicine
Medicine
Multiplex
Multiplex polymerase chain reaction
Muscular dystrophy
Phenotype
Polymerase chain reaction
Receptor