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Anna-Kaisa Anttonen

Showing results (1-10 of 36) with videos related to

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Brain : a Journal of Neurology|September 14, 2017
Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disordersAnna-Kaisa Anttonen, Anna-Elina Lehesjoki
Duodecim; Laaketieteellinen Aikakauskirja|January 12, 2016
[Fetal diagnosis from the mother's blood--noninvasive screening of chromosomal aberrations]Anna-Kaisa Anttonen, Vedran Stefanovic, Kristiina Aittomäki
Duodecim; Laaketieteellinen Aikakauskirja|October 29, 2013
[Tuberous sclerosis]Liisa Metsähonkala, Leena Valanne, Anna-Kaisa Anttonen
Journal of Perinatal Medicine|December 3, 2021
Cost of providing cell-free DNA screening for Down syndrome in Finland using different strategiesHoward Cuckle, Seppo Heinonen, Anna-Kaisa Anttonen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2025
Response to Gruzin et alRonja Hotakainen, Kaisa Kettunen, Anna-Kaisa Anttonen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2024
Estimation of carrier frequencies of autosomal and X-linked recessive genetic conditions based on gnomAD v4.0 data in different ancestriesRonja Hotakainen, Timo Järvinen, Kaisa Kettunen, et al.
Familial Cancer|May 30, 2020
Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancerPia Alhopuro, Reetta Vainionpää, Anna-Kaisa Anttonen, et al.
Clinical Case Reports|October 17, 2022
Multi-exon <i>COL5A1</i> deletion in a child with classical Ehlers-Danlos syndrome: A case report expanding the allelic spectrum and showing evidence of parental gonosomal mosaicismSonja Strang-Karlsson, Sylvia Keigwin, Anna-Kaisa Anttonen, et al.
Journal of Neurology|September 10, 2005
Myopathy is a prominent feature in Marinesco-Sjögren syndrome: A muscle computed tomography studyIbrahim Mahjneh, Anna-Kaisa Anttonen, Mirja Somer, et al.
Molecular Cytogenetics|December 7, 2025
Optical genome mapping identifies a balanced inversion disrupting DMD in a patient with Duchenne muscular dystrophyTuuni Turtinen, Pirjo Isohanni, Anna-Kaisa Anttonen, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Brain : a Journal of Neurology|September 14, 2017
Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disordersAnna-Kaisa Anttonen, Anna-Elina Lehesjoki
Duodecim; Laaketieteellinen Aikakauskirja|January 12, 2016
[Fetal diagnosis from the mother's blood--noninvasive screening of chromosomal aberrations]Anna-Kaisa Anttonen, Vedran Stefanovic, Kristiina Aittomäki
Duodecim; Laaketieteellinen Aikakauskirja|October 29, 2013
[Tuberous sclerosis]Liisa Metsähonkala, Leena Valanne, Anna-Kaisa Anttonen
Journal of Perinatal Medicine|December 3, 2021
Cost of providing cell-free DNA screening for Down syndrome in Finland using different strategiesHoward Cuckle, Seppo Heinonen, Anna-Kaisa Anttonen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2025
Response to Gruzin et alRonja Hotakainen, Kaisa Kettunen, Anna-Kaisa Anttonen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2024
Estimation of carrier frequencies of autosomal and X-linked recessive genetic conditions based on gnomAD v4.0 data in different ancestriesRonja Hotakainen, Timo Järvinen, Kaisa Kettunen, et al.
Familial Cancer|May 30, 2020
Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancerPia Alhopuro, Reetta Vainionpää, Anna-Kaisa Anttonen, et al.
Clinical Case Reports|October 17, 2022
Multi-exon <i>COL5A1</i> deletion in a child with classical Ehlers-Danlos syndrome: A case report expanding the allelic spectrum and showing evidence of parental gonosomal mosaicismSonja Strang-Karlsson, Sylvia Keigwin, Anna-Kaisa Anttonen, et al.
Journal of Neurology|September 10, 2005
Myopathy is a prominent feature in Marinesco-Sjögren syndrome: A muscle computed tomography studyIbrahim Mahjneh, Anna-Kaisa Anttonen, Mirja Somer, et al.
Molecular Cytogenetics|December 7, 2025
Optical genome mapping identifies a balanced inversion disrupting DMD in a patient with Duchenne muscular dystrophyTuuni Turtinen, Pirjo Isohanni, Anna-Kaisa Anttonen, et al.
Pageof 4