Alitalo T[au] - Search Results

Year	Number of Results
1987	2
1988	2
1989	3
1990	2
1991	3
1992	1
1995	1
1996	1
1997	1
1998	1
1999	2
2000	2
2001	1
2002	3
2003	2
2005	1
2006	2
2007	1
2013	1
2014	1
2020	1
2021	2
2022	1
2024	0

1

Duplication/triplication mosaicism of EBF3 and expansion of the EBF3 neurodevelopmental disorder phenotype.

Ignatius E, Puosi R, Palomäki M, Forsbom N, Pohjanpelto M, Alitalo T, Anttonen AK, Avela K, Haataja L, Carroll CJ, Lönnqvist T, Isohanni P. Ignatius E, et al. Among authors: alitalo t. Eur J Paediatr Neurol. 2022 Mar;37:1-7. doi: 10.1016/j.ejpn.2021.12.012. Epub 2021 Dec 26. Eur J Paediatr Neurol. 2022. PMID: 34999443 Free article.

2

Prenatal array comparative genomic hybridization in a well-defined cohort of high-risk pregnancies. A 3-year implementation results in a public tertiary academic referral hospital.

Tanner LM, Alitalo T, Stefanovic V. Tanner LM, et al. Among authors: alitalo t. Prenat Diagn. 2021 Mar;41(4):422-433. doi: 10.1002/pd.5877. Epub 2020 Dec 31. Prenat Diagn. 2021. PMID: 33340112

3

Prevalence of the fragile X syndrome in four birth cohorts of children of school age.

Kähkönen M, Alitalo T, Airaksinen E, Matilainen R, Launiala K, Autio S, Leisti J. Kähkönen M, et al. Among authors: alitalo t. Hum Genet. 1987 Sep;77(1):85-7. doi: 10.1007/BF00284720. Hum Genet. 1987. PMID: 3623561

4

Population cytogenetics of folate-sensitive fragile sites. II. Autosomal rare fragile sites.

Kähkönen M, Tengström C, Alitalo T, Matilainen R, Kaski M, Airaksinen E. Kähkönen M, et al. Among authors: alitalo t. Hum Genet. 1989 Apr;82(1):3-8. doi: 10.1007/BF00288261. Hum Genet. 1989. PMID: 2714776

5

Identification of fifteen novel PHEX gene mutations in Finnish patients with hypophosphatemic rickets.

Tyynismaa H, Kaitila I, Näntö-Salonen K, Ala-Houhala M, Alitalo T. Tyynismaa H, et al. Among authors: alitalo t. Hum Mutat. 2000 Apr;15(4):383-4. doi: 10.1002/(SICI)1098-1004(200004)15:4<383::AID-HUMU18>3.0.CO;2-#. Hum Mutat. 2000. PMID: 10737991

6

Molecular characterization of a Y;15 translocation segregating in a family.

Alitalo T, Tiihonen J, Hakola P, de la Chapelle A. Alitalo T, et al. Hum Genet. 1988 May;79(1):29-35. doi: 10.1007/BF00291705. Hum Genet. 1988. PMID: 3366460

7

Genetic variation in schlafen genes in a patient with a recapitulation of the murine Elektra phenotype.

Recher M, Karjalainen-Lindsberg ML, Lindlöf M, Söderlund-Venermo M, Lanzi G, Väisänen E, Kumar A, Sadeghi M, Berger CT, Alitalo T, Anttila P, Kolehmainen M, Franssila R, Chen T, Siitonen S, Delmonte OM, Walter JE, Pessach I, Hess C, Simpson MA, Navarini AA, Giliani S, Hedman K, Seppänen M, Notarangelo LD. Recher M, et al. Among authors: alitalo t. J Allergy Clin Immunol. 2014 May;133(5):1462-5, 1465.e1-5. doi: 10.1016/j.jaci.2013.10.052. Epub 2013 Dec 24. J Allergy Clin Immunol. 2014. PMID: 24373355 No abstract available.

8

A novel CACNA1F gene mutation causes Aland Island eye disease.

Jalkanen R, Bech-Hansen NT, Tobias R, Sankila EM, Mäntyjärvi M, Forsius H, de la Chapelle A, Alitalo T. Jalkanen R, et al. Among authors: alitalo t. Invest Ophthalmol Vis Sci. 2007 Jun;48(6):2498-502. doi: 10.1167/iovs.06-1103. Invest Ophthalmol Vis Sci. 2007. PMID: 17525176

9

A new genetic locus for X linked progressive cone-rod dystrophy.

Jalkanen R, Demirci FY, Tyynismaa H, Bech-Hansen T, Meindl A, Peippo M, Mäntyjärvi M, Gorin MB, Alitalo T. Jalkanen R, et al. Among authors: alitalo t. J Med Genet. 2003 Jun;40(6):418-23. doi: 10.1136/jmg.40.6.418. J Med Genet. 2003. PMID: 12807962 Free PMC article.

10

Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs.

Page DC, Disteche CM, Simpson EM, de la Chapelle A, Andersson M, Alitalo T, Brown LG, Green P, Akots G. Page DC, et al. Among authors: alitalo t. Genomics. 1990 May;7(1):37-46. doi: 10.1016/0888-7543(90)90516-w. Genomics. 1990. PMID: 1970799

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