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L Pulkkinen

Showing results (41-50 of 138) with videos related to

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American Journal of Medical Genetics|August 9, 1996
Deletion in the FMR1 gene in a fragile-X maleA Mannermaa, L Pulkkinen, E Kajanoja, et al.
Prenatal Diagnosis|April 1, 1997
Mutation-based prenatal diagnosis of Herlitz junctional epidermolysis bullosaA M Christiano, L Pulkkinen, J A McGrath, et al.
The New England Journal of Medicine|October 4, 1990
Location on chromosome 15 of the gene defect causing Marfan syndromeK Kainulainen, L Pulkkinen, A Savolainen, et al.
Prenatal Diagnosis|March 10, 2001
Antenatal genetic screening for congenital nephrosisJ Kallinen, S Heinonen, M Ryynänen, et al.
Nutrition & Diabetes|November 17, 2012
Microfibrillar-associated protein 5 is linked with markers of obesity-related extracellular matrix remodeling and inflammationM Vaittinen, M Kolehmainen, U Schwab, et al.
Antimicrobial Agents and Chemotherapy|January 1, 1986
Emergence of trimethoprim resistance in relation to drug consumption in a Finnish hospital from 1971 through 1984P Huovinen, L Pulkkinen, H L Helin, et al.
Terapevticheskii Arkhiv|January 1, 1986
[Markers of virulence of Yersinia enterocolitica strain 0:3 isolated from patients with and without arthritis]A Toivanen, L Pulkkinen, O P Lehtonen, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 1, 1997
Genomic organization of the integrin beta 4 gene (ITGB4): a homozygous splice-site mutation in a patient with junctional epidermolysis bullosa associated with pyloric atresiaL Pulkkinen, K Kurtz, Y Xu, et al.
Pediatric Dermatology|September 16, 2000
Epidermolysis bullosa, pyloric atresia, and obstructive uropathy: a report of two case reports with molecular correlation and clinical managementR Wallerstein, M L Klein, N Genieser, et al.
The Journal of Investigative Dermatology|September 18, 1998
Novel COL7A1 mutations in dystrophic forms of epidermolysis bullosaA Kon, L Pulkkinen, A Ishida-Yamamoto, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics|August 9, 1996
Deletion in the FMR1 gene in a fragile-X maleA Mannermaa, L Pulkkinen, E Kajanoja, et al.
Prenatal Diagnosis|April 1, 1997
Mutation-based prenatal diagnosis of Herlitz junctional epidermolysis bullosaA M Christiano, L Pulkkinen, J A McGrath, et al.
The New England Journal of Medicine|October 4, 1990
Location on chromosome 15 of the gene defect causing Marfan syndromeK Kainulainen, L Pulkkinen, A Savolainen, et al.
Prenatal Diagnosis|March 10, 2001
Antenatal genetic screening for congenital nephrosisJ Kallinen, S Heinonen, M Ryynänen, et al.
Nutrition & Diabetes|November 17, 2012
Microfibrillar-associated protein 5 is linked with markers of obesity-related extracellular matrix remodeling and inflammationM Vaittinen, M Kolehmainen, U Schwab, et al.
Antimicrobial Agents and Chemotherapy|January 1, 1986
Emergence of trimethoprim resistance in relation to drug consumption in a Finnish hospital from 1971 through 1984P Huovinen, L Pulkkinen, H L Helin, et al.
Terapevticheskii Arkhiv|January 1, 1986
[Markers of virulence of Yersinia enterocolitica strain 0:3 isolated from patients with and without arthritis]A Toivanen, L Pulkkinen, O P Lehtonen, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 1, 1997
Genomic organization of the integrin beta 4 gene (ITGB4): a homozygous splice-site mutation in a patient with junctional epidermolysis bullosa associated with pyloric atresiaL Pulkkinen, K Kurtz, Y Xu, et al.
Pediatric Dermatology|September 16, 2000
Epidermolysis bullosa, pyloric atresia, and obstructive uropathy: a report of two case reports with molecular correlation and clinical managementR Wallerstein, M L Klein, N Genieser, et al.
The Journal of Investigative Dermatology|September 18, 1998
Novel COL7A1 mutations in dystrophic forms of epidermolysis bullosaA Kon, L Pulkkinen, A Ishida-Yamamoto, et al.
Pageof 14