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Linda Siggberg

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American Journal of Medical Genetics. Part A|September 17, 2008
Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomalySirpa Ala-Mello, Linda Siggberg, Sakari Knuutila, et al.
Orphanet Journal of Rare Diseases|June 23, 2011
9q22 Deletion--first familial caseLinda Siggberg, Maarit Peippo, Marjatta Sipponen, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patientsLinda Siggberg, Sirpa Ala-Mello, Elisa Jaakkola, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activityLinda Siggberg, Aki Mustonen, Robert Schuit, et al.
BMC Medical Genetics|May 1, 2015
Erratum to: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH resultLinda Siggberg, Sirpa Ala-Mello, Tarja Linnankivi, et al.
BMC Medical Genetics|September 19, 2012
High-resolution SNP array analysis of patients with developmental disorder and normal array CGH resultsLinda Siggberg, Sirpa Ala-Mello, Ala-Mello Sirpa, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|September 17, 2008
Further evidence for a relationship between the 5p15 chromosome region and the oculoauriculovertebral anomalySirpa Ala-Mello, Linda Siggberg, Sakari Knuutila, et al.
Orphanet Journal of Rare Diseases|June 23, 2011
9q22 Deletion--first familial caseLinda Siggberg, Maarit Peippo, Marjatta Sipponen, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patientsLinda Siggberg, Sirpa Ala-Mello, Elisa Jaakkola, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2011
Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activityLinda Siggberg, Aki Mustonen, Robert Schuit, et al.
BMC Medical Genetics|May 1, 2015
Erratum to: High-resolution SNP array analysis of patients with developmental disorder and normal array CGH resultLinda Siggberg, Sirpa Ala-Mello, Tarja Linnankivi, et al.
BMC Medical Genetics|September 19, 2012
High-resolution SNP array analysis of patients with developmental disorder and normal array CGH resultsLinda Siggberg, Sirpa Ala-Mello, Ala-Mello Sirpa, et al.
Pageof 1