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

Year Number of Results
1991 1
1993 1
1994 3
1996 1
1997 2
1998 1
2001 2
2003 3
2004 5
2005 3
2006 2
2007 1
2008 1
2009 1
2013 1
2014 1
2015 3
2016 2
2017 1
2019 2
2024 0

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34 results

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Page 1
Microdeletion 22q11 in complex cardiovascular malformations.
Mehraein Y, Wippermann CF, Michel-Behnke I, Nhan Ngo TK, Hillig U, Giersberg M, Aulepp U, Barth H, Fritz B, Rehder H. Mehraein Y, et al. Hum Genet. 1997 Apr;99(4):433-42. doi: 10.1007/s004390050385. Hum Genet. 1997. PMID: 9099830
A new familial case of microdeletion syndrome 10p15.3.
Eggert M, Müller S, Heinrich U, Mehraein Y. Eggert M, et al. Among authors: mehraein y. Eur J Med Genet. 2016 Apr;59(4):179-82. doi: 10.1016/j.ejmg.2016.02.008. Epub 2016 Feb 24. Eur J Med Genet. 2016. PMID: 26921531
PORCN mutations in focal dermal hypoplasia: coping with lethality.
Bornholdt D, Oeffner F, König A, Happle R, Alanay Y, Ascherman J, Benke PJ, Boente Mdel C, van der Burgt I, Chassaing N, Ellis I, Francisco CR, Della Giovanna P, Hamel B, Has C, Heinelt K, Janecke A, Kastrup W, Loeys B, Lohrisch I, Marcelis C, Mehraein Y, Nicolas ME, Pagliarini D, Paradisi M, Patrizi A, Piccione M, Piza-Katzer H, Prager B, Prescott K, Strien J, Utine GE, Zeller MS, Grzeschik KH. Bornholdt D, et al. Among authors: mehraein y. Hum Mutat. 2009 May;30(5):E618-28. doi: 10.1002/humu.20992. Hum Mutat. 2009. PMID: 19309688
Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders.
Geis T, Rödl T, Topaloğlu H, Balci-Hayta B, Hinreiner S, Müller-Felber W, Schoser B, Mehraein Y, Hübner A, Zirn B, Hoopmann M, Reutter H, Mowat D, Schuierer G, Schara U, Hehr U, Kölbel H. Geis T, et al. Among authors: mehraein y. Orphanet J Rare Dis. 2019 Jul 16;14(1):179. doi: 10.1186/s13023-019-1119-0. Orphanet J Rare Dis. 2019. PMID: 31311558 Free PMC article.
34 results