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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1955 1
1985 2
1987 1
1988 2
1989 2
1992 3
1993 2
1994 1
1995 1
1996 3
1997 2
1998 7
1999 5
2000 5
2001 8
2002 9
2003 4
2004 4
2005 6
2006 4
2007 5
2008 9
2009 5
2010 4
2011 2
2012 4
2013 5
2014 4
2015 2
2016 5
2017 7
2018 4
2019 5
2020 5
2021 6
2022 4
2023 1
2024 0

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Similar articles for PMID: 10332035

137 results

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Page 1
Correlations of genotype and phenotype in hypophosphatasia.
Zurutuza L, Muller F, Gibrat JF, Taillandier A, Simon-Bouy B, Serre JL, Mornet E. Zurutuza L, et al. Hum Mol Genet. 1999 Jun;8(6):1039-46. doi: 10.1093/hmg/8.6.1039. Hum Mol Genet. 1999. PMID: 10332035
A molecular approach to dominance in hypophosphatasia.
Lia-Baldini AS, Muller F, Taillandier A, Gibrat JF, Mouchard M, Robin B, Simon-Bouy B, Serre JL, Aylsworth AS, Bieth E, Delanote S, Freisinger P, Hu JC, Krohn HP, Nunes ME, Mornet E. Lia-Baldini AS, et al. Hum Genet. 2001 Jul;109(1):99-108. doi: 10.1007/s004390100546. Hum Genet. 2001. PMID: 11479741
Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia.
Taillandier A, Lia-Baldini AS, Mouchard M, Robin B, Muller F, Simon-Bouy B, Serre JL, Bera-Louville A, Bonduelle M, Eckhardt J, Gaillard D, Myhre AG, Körtge-Jung S, Larget-Piet L, Malou E, Sillence D, Temple IK, Viot G, Mornet E. Taillandier A, et al. Hum Mutat. 2001;18(1):83-4. doi: 10.1002/humu.1154. Hum Mutat. 2001. PMID: 11438998
137 results