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

Year Number of Results
1981 3
1982 2
1983 4
1984 1
1985 2
1986 4
1988 4
1989 1
1991 4
1992 5
1993 2
1994 2
1995 5
1996 2
1997 4
1998 4
1999 1
2000 2
2001 1
2002 2
2003 3
2004 1
2005 4
2006 3
2008 3
2009 6
2010 3
2012 5
2013 6
2014 3
2015 4
2016 3
2017 1
2019 1
2024 0

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90 results

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Page 1
Interstitial deletion (6)q13q15.
Gershoni-Baruch R, Mandel H, Bar El H, Bar-Nizan N, Borochowitz Z, Dar H. Gershoni-Baruch R, et al. Among authors: borochowitz z. Am J Med Genet. 1996 Apr 24;62(4):345-7. doi: 10.1002/(SICI)1096-8628(19960424)62:4<345::AID-AJMG4>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8723062 Review.
Mutations in DDR2 gene cause SMED with short limbs and abnormal calcifications.
Bargal R, Cormier-Daire V, Ben-Neriah Z, Le Merrer M, Sosna J, Melki J, Zangen DH, Smithson SF, Borochowitz Z, Belostotsky R, Raas-Rothschild A. Bargal R, et al. Among authors: borochowitz z. Am J Hum Genet. 2009 Jan;84(1):80-4. doi: 10.1016/j.ajhg.2008.12.004. Epub 2008 Dec 24. Am J Hum Genet. 2009. PMID: 19110212 Free PMC article.
SMPD1 mutations and Parkinson disease.
Dagan E, Adir V, Schlesinger I, Borochowitz Z, Ayoub M, Mory A, Nassar M, Kurolap A, Aharon-Peretz J, Gershoni-Baruch R. Dagan E, et al. Among authors: borochowitz z. Parkinsonism Relat Disord. 2015 Oct;21(10):1296-7. doi: 10.1016/j.parkreldis.2015.08.019. Epub 2015 Aug 20. Parkinsonism Relat Disord. 2015. PMID: 26318962 No abstract available.
Nosology of omodysplasia.
Borochowitz Z, Barak M, Hershkowitz S. Borochowitz Z, et al. Am J Med Genet. 1995 Sep 25;58(4):377-8. doi: 10.1002/ajmg.1320580416. Am J Med Genet. 1995. PMID: 8533851 No abstract available.
Gain-of-function mutation of microRNA-140 in human skeletal dysplasia.
Grigelioniene G, Suzuki HI, Taylan F, Mirzamohammadi F, Borochowitz ZU, Ayturk UM, Tzur S, Horemuzova E, Lindstrand A, Weis MA, Grigelionis G, Hammarsjö A, Marsk E, Nordgren A, Nordenskjöld M, Eyre DR, Warman ML, Nishimura G, Sharp PA, Kobayashi T. Grigelioniene G, et al. Among authors: borochowitz zu. Nat Med. 2019 Apr;25(4):583-590. doi: 10.1038/s41591-019-0353-2. Epub 2019 Feb 25. Nat Med. 2019. PMID: 30804514 Free PMC article.
Founder mutation for Huntington disease in Caucasus Jews.
Melamed O, Behar DM, Bram C, Magal N, Pras E, Reznik-Wolf H, Borochowitz ZU, Davidov B, Mor-Cohen R, Baris HN. Melamed O, et al. Among authors: borochowitz zu. Clin Genet. 2015 Feb;87(2):167-72. doi: 10.1111/cge.12344. Epub 2014 Feb 4. Clin Genet. 2015. PMID: 24405192
Sleep apnea in fragile X syndrome.
Tirosh E, Borochowitz Z. Tirosh E, et al. Among authors: borochowitz z. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):124-7. doi: 10.1002/ajmg.1320430119. Am J Med Genet. 1992. PMID: 1605180
90 results