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Hannele Koillinen

Showing results (1-10 of 15) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|April 4, 2009
[Mitochondrial disorder underlying headache symptoms]Hannele Koillinen, Satu Jääskeläinen, Kari Koski
Duodecim; Laaketieteellinen Aikakauskirja|April 15, 2014
[How to recognize neurofibromatosis?]Sirkku Peltonen, Minna Pöyhönen, Hannele Koillinen, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalitiesMaila Penttinen, Hannele Koillinen, Harri Niinikoski, et al.
Cardiovascular Revascularization Medicine : Including Molecular Interventions|April 30, 2025
Supravalvular aortic stenosis - Novel pathogenic ELN variant in siblings with a wide spectrum of clinical cardiovascular features and a long follow-up from infancy to adulthoodSini Keskinen, Jussi Niemelä, Hannele Koillinen, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
Interstitial microdeletion of 17q11.2 is associated with hypotonia, fatigue, intellectual disability, and a subtle facial phenotype in three unrelated patientsDeborah Osio, Julia Rankin, Hannele Koillinen, et al.
Journal of Clinical Immunology|November 16, 2013
Terminal deletion of 11q with significant late-onset combined immune deficiencyMikko Seppänen, Hannele Koillinen, Satu Mustjoki, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 19, 2023
Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the DiseaseSini Keskinen, Teija Paakkola, Mirjami Mattila, et al.
European Journal of Human Genetics : EJHG|September 15, 2005
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndromeMyriam Peyrard-Janvid, Marie Pegelow, Hannele Koillinen, et al.
European Heart Journal|June 19, 2015
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathyOyediran Akinrinade, Laura Ollila, Sanna Vattulainen, et al.
European Journal of Human Genetics : EJHG|April 4, 2003
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathiaMiia Melkoniemi, Hannele Koillinen, Minna Männikkö, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Duodecim; Laaketieteellinen Aikakauskirja|April 4, 2009
[Mitochondrial disorder underlying headache symptoms]Hannele Koillinen, Satu Jääskeläinen, Kari Koski
Duodecim; Laaketieteellinen Aikakauskirja|April 15, 2014
[How to recognize neurofibromatosis?]Sirkku Peltonen, Minna Pöyhönen, Hannele Koillinen, et al.
American Journal of Medical Genetics. Part A|February 12, 2009
Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalitiesMaila Penttinen, Hannele Koillinen, Harri Niinikoski, et al.
Cardiovascular Revascularization Medicine : Including Molecular Interventions|April 30, 2025
Supravalvular aortic stenosis - Novel pathogenic ELN variant in siblings with a wide spectrum of clinical cardiovascular features and a long follow-up from infancy to adulthoodSini Keskinen, Jussi Niemelä, Hannele Koillinen, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
Interstitial microdeletion of 17q11.2 is associated with hypotonia, fatigue, intellectual disability, and a subtle facial phenotype in three unrelated patientsDeborah Osio, Julia Rankin, Hannele Koillinen, et al.
Journal of Clinical Immunology|November 16, 2013
Terminal deletion of 11q with significant late-onset combined immune deficiencyMikko Seppänen, Hannele Koillinen, Satu Mustjoki, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 19, 2023
Prenatal Coffin-Siris Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the DiseaseSini Keskinen, Teija Paakkola, Mirjami Mattila, et al.
European Journal of Human Genetics : EJHG|September 15, 2005
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndromeMyriam Peyrard-Janvid, Marie Pegelow, Hannele Koillinen, et al.
European Heart Journal|June 19, 2015
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathyOyediran Akinrinade, Laura Ollila, Sanna Vattulainen, et al.
European Journal of Human Genetics : EJHG|April 4, 2003
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathiaMiia Melkoniemi, Hannele Koillinen, Minna Männikkö, et al.
Pageof 2