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M Peippo

Showing results (1-10 of 23) with videos related to

Pageof 3
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Molecular Syndromology|June 7, 2012
Pitt-Hopkins SyndromeM Peippo, J Ignatius
Clinical Dysmorphology|January 1, 1996
Two more diagnostic signs in the Floating-Harbor syndromeS Ala-Mello, M Peippo
Clinical Genetics|January 24, 1998
Applicability of a checklist for clinical screening of the fragile X syndromeM Arvio, M Peippo, K O Simola
The Journal of Pediatrics|February 15, 2001
Bone marrow transplantation for aspartylglucosaminuria: follow-up study of transplanted and non-transplanted patientsM Arvio, O Sauna-Aho, M Peippo
Pediatric Hematology and Oncology|July 1, 1994
Hemophilia A: experiences and attitudes of mothers, sisters, and daughtersS Ranta, A E Lehesjoki, M Peippo, et al.
American Journal of Medical Genetics|July 15, 1994
FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardationH von Koskull, N Gahmberg, R Salonen, et al.
Acta Ophthalmologica Scandinavica|July 17, 2001
Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophyM Mäntyjärvi, P Nurmenniemi, J Partanen, et al.
American Journal of Medical Genetics|November 15, 1992
Cardio-facio-cutaneous syndrome: three additional cases and review of the literatureM Somer, M Peippo, K Aalto-Korte, et al.
Clinical Dysmorphology|May 7, 2004
Dysmorphic facial features in aspartylglucosaminuria patients and carriersMaria A Arvio, Maarit M Peippo, Pekka J Arvio, et al.
Neurology|August 28, 2002
Valproate embryopathy in three sets of siblings: further proof of hereditary susceptibilityH Malm, E Kajantie, S Kivirikko, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Molecular Syndromology|June 7, 2012
Pitt-Hopkins SyndromeM Peippo, J Ignatius
Clinical Dysmorphology|January 1, 1996
Two more diagnostic signs in the Floating-Harbor syndromeS Ala-Mello, M Peippo
Clinical Genetics|January 24, 1998
Applicability of a checklist for clinical screening of the fragile X syndromeM Arvio, M Peippo, K O Simola
The Journal of Pediatrics|February 15, 2001
Bone marrow transplantation for aspartylglucosaminuria: follow-up study of transplanted and non-transplanted patientsM Arvio, O Sauna-Aho, M Peippo
Pediatric Hematology and Oncology|July 1, 1994
Hemophilia A: experiences and attitudes of mothers, sisters, and daughtersS Ranta, A E Lehesjoki, M Peippo, et al.
American Journal of Medical Genetics|July 15, 1994
FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardationH von Koskull, N Gahmberg, R Salonen, et al.
Acta Ophthalmologica Scandinavica|July 17, 2001
Clinical features and a follow-up study in a family with X-linked progressive cone-rod dystrophyM Mäntyjärvi, P Nurmenniemi, J Partanen, et al.
American Journal of Medical Genetics|November 15, 1992
Cardio-facio-cutaneous syndrome: three additional cases and review of the literatureM Somer, M Peippo, K Aalto-Korte, et al.
Clinical Dysmorphology|May 7, 2004
Dysmorphic facial features in aspartylglucosaminuria patients and carriersMaria A Arvio, Maarit M Peippo, Pekka J Arvio, et al.
Neurology|August 28, 2002
Valproate embryopathy in three sets of siblings: further proof of hereditary susceptibilityH Malm, E Kajantie, S Kivirikko, et al.
Pageof 3