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D Lindhout

Showing results (71-80 of 123) with videos related to

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Journal of Medical Genetics|January 1, 1997
Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumbJ Zguricas, P F Dijkstra, E S Gelsema, et al.
International Orthopaedics|June 20, 2002
Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-upA K Mostert, B R H Jansen, P F Dijkstra, et al.
Diabetologia|August 1, 1988
Fibroblasts from a leprechaun patient have defects in insulin binding and insulin receptor autophosphorylationJ A Maassen, M P Klinkhamer, G C van der Zon, et al.
Human Genetics|October 1, 1994
Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis familiesB Janssen, J Sampson, M van der Est, et al.
Nature Genetics|December 8, 1998
MSH2 genomic deletions are a frequent cause of HNPCCJ Wijnen, H van der Klift, H Vasen, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.
The EMBO Journal|September 1, 1989
A leucine-to-proline mutation in the insulin receptor in a family with insulin resistanceM P Klinkhamer, N A Groen, G C van der Zon, et al.
Journal of Medical Genetics|May 5, 1999
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlationM van Slegtenhorst, S Verhoef, A Tempelaars, et al.
Genomics|July 1, 1994
Genetic heterogeneity of familial hemiplegic migraineR A Ophoff, R van Eijk, L A Sandkuijl, et al.
Annals of the New York Academy of Sciences|January 1, 1991
A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23L A Janssen, S Povey, J Attwood, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
Journal of Medical Genetics|January 1, 1997
Metacarpophalangeal pattern (MCPP) profile analysis in a family with triphalangeal thumbJ Zguricas, P F Dijkstra, E S Gelsema, et al.
International Orthopaedics|June 20, 2002
Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-upA K Mostert, B R H Jansen, P F Dijkstra, et al.
Diabetologia|August 1, 1988
Fibroblasts from a leprechaun patient have defects in insulin binding and insulin receptor autophosphorylationJ A Maassen, M P Klinkhamer, G C van der Zon, et al.
Human Genetics|October 1, 1994
Refined localization of TSC1 by combined analysis of 9q34 and 16p13 data in 14 tuberous sclerosis familiesB Janssen, J Sampson, M van der Est, et al.
Nature Genetics|December 8, 1998
MSH2 genomic deletions are a frequent cause of HNPCCJ Wijnen, H van der Klift, H Vasen, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.
The EMBO Journal|September 1, 1989
A leucine-to-proline mutation in the insulin receptor in a family with insulin resistanceM P Klinkhamer, N A Groen, G C van der Zon, et al.
Journal of Medical Genetics|May 5, 1999
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlationM van Slegtenhorst, S Verhoef, A Tempelaars, et al.
Genomics|July 1, 1994
Genetic heterogeneity of familial hemiplegic migraineR A Ophoff, R van Eijk, L A Sandkuijl, et al.
Annals of the New York Academy of Sciences|January 1, 1991
A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23L A Janssen, S Povey, J Attwood, et al.
Pageof 13