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

Year Number of Results
1969 1
2001 1
2002 3
2003 4
2005 2
2006 5
2007 1
2008 2
2009 1
2020 1
2023 0

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20 results

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Page 1
DHPLC mutation analysis of phenylketonuria.
Bräutigam S, Kujat A, Kirst P, Seidel J, Lüleyap HU, Froster UG. Bräutigam S, et al. Among authors: kujat a. Mol Genet Metab. 2003 Mar;78(3):205-10. doi: 10.1016/s1096-7192(02)00228-7. Mol Genet Metab. 2003. PMID: 12649065
Renal malformations in deletion 22q11.2 patients.
Kujat A, Schulz MD, Strenge S, Froster UG. Kujat A, et al. Am J Med Genet A. 2006 Jul 15;140(14):1601-2. doi: 10.1002/ajmg.a.31289. Am J Med Genet A. 2006. PMID: 16761295 No abstract available.
Parental mosaicism of JAG1 mutations in families with Alagille syndrome.
Giannakudis J, Röpke A, Kujat A, Krajewska-Walasek M, Hughes H, Fryns JP, Bankier A, Amor D, Schlicker M, Hansmann I. Giannakudis J, et al. Among authors: kujat a. Eur J Hum Genet. 2001 Mar;9(3):209-16. doi: 10.1038/sj.ejhg.5200613. Eur J Hum Genet. 2001. PMID: 11313761
Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome.
Heinritz W, Moschik A, Kujat A, Spranger S, Heilbronner H, Demuth S, Bier A, Tihanyi M, Mundlos S, Gruenauer-Kloevekorn C, Froster UG. Heinritz W, et al. Among authors: kujat a. Heart. 2005 Mar;91(3):383-4. doi: 10.1136/hrt.2004.036855. Heart. 2005. PMID: 15710732 Free PMC article. No abstract available.
20 results