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Results by year

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

Year Number of Results
1992 3
1993 7
1994 1
1995 3
1996 4
1997 1
1998 2
1999 3
2000 3
2001 7
2002 10
2003 6
2004 6
2005 8
2006 9
2007 3
2008 8
2009 8
2010 3
2011 1
2012 1
2013 1
2018 1
2023 0

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94 results

Results by year

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Page 1
Diaphragmatic hernia in 18p- syndrome.
Strenge S, Froster UG. Strenge S, et al. Among authors: froster ug. Am J Med Genet A. 2004 Feb 15;125A(1):97-9. doi: 10.1002/ajmg.a.20459. Am J Med Genet A. 2004. PMID: 14755475 Review. No abstract available.
[Genetic risks of in vitro fertilization].
Froster UG. Froster UG. Geburtshilfe Frauenheilkd. 1995 Mar;55(3):121-6. doi: 10.1055/s-2007-1022788. Geburtshilfe Frauenheilkd. 1995. PMID: 7665057 Review. German.
[Current aspects of the diagnosis of malignant hyperthermia].
Rüffert H, Olthoff D, Deutrich C, Froster UG. Rüffert H, et al. Among authors: froster ug. Anaesthesist. 2002 Nov;51(11):904-13. doi: 10.1007/s00101-002-0390-x. Anaesthesist. 2002. PMID: 12434264 Review. German.
De novo complete trisomy 5p: clinical report and FISH studies.
Reichenbach H, Holland H, Dalitz E, Demandt C, Meiner A, Chudoba I, Lemke J, Claussen U, Froster UG. Reichenbach H, et al. Among authors: froster ug. Am J Med Genet. 1999 Aug 27;85(5):447-51. doi: 10.1002/(sici)1096-8628(19990827)85:5<447::aid-ajmg3>;2-5. Am J Med Genet. 1999. PMID: 10405440 Review.
DHPLC mutation analysis of phenylketonuria.
Bräutigam S, Kujat A, Kirst P, Seidel J, Lüleyap HU, Froster UG. Bräutigam S, et al. Among authors: froster ug. 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. Among authors: froster ug. 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.
Trisomy of 5p and marker chromosomes.
Froster UG, Reichenbach H. Froster UG, et al. Am J Med Genet. 2000 Jul 3;93(1):76. doi: 10.1002/1096-8628(20000703)93:1<76::aid-ajmg13>;2-g. Am J Med Genet. 2000. PMID: 10861686 No abstract available.
The human TBX5 gene mutation database.
Heinritz W, Shou L, Moschik A, Froster UG. Heinritz W, et al. Among authors: froster ug. Hum Mutat. 2005 Oct;26(4):397. doi: 10.1002/humu.9375. Hum Mutat. 2005. PMID: 16134140
Cysteine-sparing notch3 mutations: cadasil or cadasil variants?
Scheid R, Heinritz W, Leyhe T, Thal DR, Schober R, Strenge S, von Cramon DY, Froster UG. Scheid R, et al. Among authors: froster ug. Neurology. 2008 Sep 2;71(10):774-6. doi: 10.1212/01.wnl.0000324928.44694.f7. Neurology. 2008. PMID: 18765654 No abstract available.
94 results