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

Year Number of Results
1991 1
1992 1
1993 3
1994 3
1995 2
1996 3
1997 2
1998 2
2001 1
2004 1
2006 1
2007 1
2008 1
2011 2
2012 1
2014 1
2021 1
2023 0

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26 results

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Page 1
Molecular basis for nonphenylketonuria hyperphenylalaninemia.
Economou-Petersen E, Henriksen KF, Guldberg P, Güttler F. Economou-Petersen E, et al. Among authors: henriksen kf. Genomics. 1992 Sep;14(1):1-5. doi: 10.1016/s0888-7543(05)80274-5. Genomics. 1992. PMID: 1358789
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B.
Halgren C, Kjaergaard S, Bak M, Hansen C, El-Schich Z, Anderson CM, Henriksen KF, Hjalgrim H, Kirchhoff M, Bijlsma EK, Nielsen M, den Hollander NS, Ruivenkamp CA, Isidor B, Le Caignec C, Zannolli R, Mucciolo M, Renieri A, Mari F, Anderlid BM, Andrieux J, Dieux A, Tommerup N, Bache I. Halgren C, et al. Among authors: henriksen kf. Clin Genet. 2012 Sep;82(3):248-55. doi: 10.1111/j.1399-0004.2011.01755.x. Epub 2011 Aug 24. Clin Genet. 2012. PMID: 21801163 Free PMC article.
Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2.
Jakobsen LP, Ullmann R, Christensen SB, Jensen KE, Mølsted K, Henriksen KF, Hansen C, Knudsen MA, Larsen LA, Tommerup N, Tümer Z. Jakobsen LP, et al. Among authors: henriksen kf. J Med Genet. 2007 Jun;44(6):381-6. doi: 10.1136/jmg.2006.046177. J Med Genet. 2007. PMID: 17551083 Free PMC article.
26 results