Similar articles for PMID: 10090893

Year	Number of Results
1990	1
1992	2
1993	4
1995	5
1996	5
1997	9
1998	6
1999	12
2000	15
2001	7
2002	5
2003	12
2004	8
2005	8
2006	6
2007	12
2008	10
2009	3
2010	2
2011	5
2012	5
2013	2
2014	3
2015	3
2016	2
2017	1
2018	3
2019	3
2020	4
2021	1
2022	1
2024	0

1

Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

Edelmann L, Pandita RK, Morrow BE. Edelmann L, et al. Am J Hum Genet. 1999 Apr;64(4):1076-86. doi: 10.1086/302343. Am J Hum Genet. 1999. PMID: 10090893 Free PMC article.

2

Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.

Funke B, Edelmann L, McCain N, Pandita RK, Ferreira J, Merscher S, Zohouri M, Cannizzaro L, Shanske A, Morrow BE. Funke B, et al. Am J Hum Genet. 1999 Mar;64(3):747-58. doi: 10.1086/302284. Am J Hum Genet. 1999. PMID: 10053009 Free PMC article.

3

Investigation of meiotic rearrangements in DGS/VCFS patients with a microdeletion 22q11.2.

Trost D, Wiebe W, Uhlhaas S, Schwindt P, Schwanitz G. Trost D, et al. J Med Genet. 2000 Jun;37(6):452-4. doi: 10.1136/jmg.37.6.452. J Med Genet. 2000. PMID: 10928854 Free PMC article. No abstract available.

4

Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

Morrow B, Goldberg R, Carlson C, Das Gupta R, Sirotkin H, Collins J, Dunham I, O'Donnell H, Scambler P, Shprintzen R, et al. Morrow B, et al. Am J Hum Genet. 1995 Jun;56(6):1391-403. Am J Hum Genet. 1995. PMID: 7762562 Free PMC article.

5

Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.

Shaikh TH, O'Connor RJ, Pierpont ME, McGrath J, Hacker AM, Nimmakayalu M, Geiger E, Emanuel BS, Saitta SC. Shaikh TH, et al. Genome Res. 2007 Apr;17(4):482-91. doi: 10.1101/gr.5986507. Epub 2007 Mar 9. Genome Res. 2007. PMID: 17351135 Free PMC article.

6

Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients.

Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, Patanjali SR, Weissman SM, Anyane-Yeboa K, Warburton D, Scambler P, Shprintzen R, Kucherlapati R, Morrow BE. Carlson C, et al. Am J Hum Genet. 1997 Sep;61(3):620-9. doi: 10.1086/515508. Am J Hum Genet. 1997. PMID: 9326327 Free PMC article.

7

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.

Bittel DC, Yu S, Newkirk H, Kibiryeva N, Holt A 3rd, Butler MG, Cooley LD. Bittel DC, et al. Cytogenet Genome Res. 2009;124(2):113-20. doi: 10.1159/000207515. Epub 2009 May 5. Cytogenet Genome Res. 2009. PMID: 19420922 Free PMC article.

8

A common molecular basis for rearrangement disorders on chromosome 22q11.

Edelmann L, Pandita RK, Spiteri E, Funke B, Goldberg R, Palanisamy N, Chaganti RS, Magenis E, Shprintzen RJ, Morrow BE. Edelmann L, et al. Hum Mol Genet. 1999 Jul;8(7):1157-67. doi: 10.1093/hmg/8.7.1157. Hum Mol Genet. 1999. PMID: 10369860

9

AT-rich palindromes mediate the constitutional t(11;22) translocation.

Edelmann L, Spiteri E, Koren K, Pulijaal V, Bialer MG, Shanske A, Goldberg R, Morrow BE. Edelmann L, et al. Am J Hum Genet. 2001 Jan;68(1):1-13. doi: 10.1086/316952. Epub 2000 Nov 28. Am J Hum Genet. 2001. PMID: 11095996 Free PMC article.

10

22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.

Ben-Shachar S, Ou Z, Shaw CA, Belmont JW, Patel MS, Hummel M, Amato S, Tartaglia N, Berg J, Sutton VR, Lalani SR, Chinault AC, Cheung SW, Lupski JR, Patel A. Ben-Shachar S, et al. Am J Hum Genet. 2008 Jan;82(1):214-21. doi: 10.1016/j.ajhg.2007.09.014. Am J Hum Genet. 2008. PMID: 18179902 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

155 results

Results by year