drs. P.C. (Petra) Kramer

docent Nederlands / NT2

Faculteit der Letteren

Telefoon:

06 2474 8291

E-mail:

p.c.kramer rug.nl

Research Portal

Publicaties

Acrocapitofemoral dysplasia: an autosomal recessive skeletal dysplasia with cone shaped epiphyses in the hands and hips

Mortier, G., Kramer, P., Giedion, A. & Beemer, F., mrt.-2003, In: Journal of Medical Genetics. 40, 3, blz. 201-207 7 blz.

Onderzoeksoutput › › peer review

Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone- shaped epiphyses in hands and hips

Hellemans, J., Coucke, P., Giedion, A., De Paepe, A., Kramer, P., Beemer, F. & Mortier, G., apr.-2003, In: American Journal of Human Genetics. 72, 4, blz. 1040-1046 7 blz.

Onderzoeksoutput › › peer review

Displacement response of juvenile arthritic wrists during grasp

Helders, P. J., Nieuwenhuis, M. K., van der Net, J., Kramer, P. P., Kuis, W. & Buchanan, T. S., dec.-2000, In: Arthritis Care and Research. 13, 6, blz. 375-81 7 blz.

Onderzoeksoutput › › peer review

A GENE FOR EPISODIC ATAXIA/MYOKYMIA MAPS TO CHROMOSOME 12P13

LITT, M., KRAMER, P., BROWNE, D., GANCHER, S., BRUNT, E., ROOT, D., PHROMCHOTIKUL, T., DUBAY, C. & NUTT, J., okt.-1994, In: American Journal of Human Genetics. 55, 4, blz. 702-709 8 blz.

Onderzoeksoutput › › peer review

EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE, KCNA1

BROWNE, D., GANCHER, S., NUTT, J., BRUNT, E., SMITH, E., KRAMER, P. & LITT, M., okt.-1994, In: Nature Genetics. 8, 2, blz. 136-140 5 blz.

Onderzoeksoutput › › peer review

INHIBITION OF 1ST OVULATION - ADMINISTRATION OF AN LHRH ANTAGONIST TO IMMATURE FEMALE RATS

MEIJSROELOFS, H., KRAMER, P., VANCAPPELLEN, W. & SCHUILING, G., mrt.-1987, In: Journal of endocrinology. 112, 3, blz. 407-415 9 blz.

Onderzoeksoutput › › peer review

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