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American Journal of Medical Genetics. Part A|September 21, 2004
The first Finnish patient with the Floating-Harbor syndrome: the follow-up of eight yearsSirpa Ala-Mello, Maarit Peippo
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|February 19, 2010
Chromosomal abnormalities in Finnish orofacial cleft patients: excess of submucous cleft patients?Tuomas Klockars, Sirpa Ala-Mello, Jorma Rautio
International Journal of Pediatric Otorhinolaryngology|September 18, 2007
Inheritance of microtia in the Finnish populationTuomas Klockars, Samuli Suutarla, Erna Kentala, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 25, 2010
Epilepsy caused by CDKL5 mutationsMaija Castrén, Eija Gaily, Carola Tengström, et al.
International Journal of Pediatric Otorhinolaryngology|June 6, 2007
Microtia in Finland: comparison of characteristics in different populationsSamuli Suutarla, Jorma Rautio, Annukka Ritvanen, et al.
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.
Duodecim; Laaketieteellinen Aikakauskirja|June 13, 2009
[Microtia--not just an ear problem]Tuomas Klockars, Erna Kentala, Kirsti Hurmerinta, et al.
Frontiers in Pediatrics|October 21, 2022
Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndromePetra Loid, Marita Lipsanen-Nyman, Sirpa Ala-Mello, 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.
JBMR Plus|August 22, 2022
Mosaic Deletions of Known Genes Explain Skeletal Dysplasias With High and Low Bone MassMari Muurinen, Fulya Taylan, Symeon Tournis, et al.
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