2p15-16.1 microdeletion syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "2p15-16.1 microdeletion syndrome" in English language version.

refsWebsite

Global rank English rank

7nih.gov

4^th place

5doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

1sanger.ac.uk

low place

doi.org

Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME (2007). "Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1". J Med Genet. 44 (4): 269–76. doi:10.1136/jmg.2006.045013. PMC 2598046. PMID 16963482.
de Leeuw N, Pfundt R, Koolen DA, Neefs I, Scheltinga I, Mieloo H, Sistermans EA, Nillesen W, Smeets DF, de Vries BB, Knoers NV (2008). "A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis". J Med Genet. 45 (2): 122–4. doi:10.1136/jmg.2007.054049. PMID 18245392. S2CID 972258.
Chabchoub E, Vermeesch JR, de Ravel T, de Cock P, Fryns JP (2008). "The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15". J Med Genet. 45 (3): 189–92. doi:10.1136/jmg.2007.056176. PMID 18310269. S2CID 32961901.
Liang JS, Shimojima K, Ohno K, Sugiura C, Une Y, Ohno K, et al. (2009). "A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion". J Med Genet. 46 (9): 645–7. doi:10.1136/jmg.2008.059220. PMID 19724011. S2CID 5128199.
Félix TM, Petrin AL, Sanseverino MT, Murray JC (2010). "Further characterization of microdeletion syndrome involving 2p15-p16.1". Am J Med Genet A. 152A (10): 2604–8. doi:10.1002/ajmg.a.33612. PMC 2946431. PMID 20799320.

nih.gov

pubmed.ncbi.nlm.nih.gov

Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME (2007). "Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1". J Med Genet. 44 (4): 269–76. doi:10.1136/jmg.2006.045013. PMC 2598046. PMID 16963482.
de Leeuw N, Pfundt R, Koolen DA, Neefs I, Scheltinga I, Mieloo H, Sistermans EA, Nillesen W, Smeets DF, de Vries BB, Knoers NV (2008). "A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis". J Med Genet. 45 (2): 122–4. doi:10.1136/jmg.2007.054049. PMID 18245392. S2CID 972258.
Chabchoub E, Vermeesch JR, de Ravel T, de Cock P, Fryns JP (2008). "The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15". J Med Genet. 45 (3): 189–92. doi:10.1136/jmg.2007.056176. PMID 18310269. S2CID 32961901.
Liang JS, Shimojima K, Ohno K, Sugiura C, Une Y, Ohno K, et al. (2009). "A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion". J Med Genet. 46 (9): 645–7. doi:10.1136/jmg.2008.059220. PMID 19724011. S2CID 5128199.
Félix TM, Petrin AL, Sanseverino MT, Murray JC (2010). "Further characterization of microdeletion syndrome involving 2p15-p16.1". Am J Med Genet A. 152A (10): 2604–8. doi:10.1002/ajmg.a.33612. PMC 2946431. PMID 20799320.

ncbi.nlm.nih.gov

Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME (2007). "Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1". J Med Genet. 44 (4): 269–76. doi:10.1136/jmg.2006.045013. PMC 2598046. PMID 16963482.
Félix TM, Petrin AL, Sanseverino MT, Murray JC (2010). "Further characterization of microdeletion syndrome involving 2p15-p16.1". Am J Med Genet A. 152A (10): 2604–8. doi:10.1002/ajmg.a.33612. PMC 2946431. PMID 20799320.

sanger.ac.uk

decipher.sanger.ac.uk

"2p15-16.1 microdeletion syndrome". Wellcome Trust Sanger Institute. Retrieved 24 May 2011.

semanticscholar.org

api.semanticscholar.org

de Leeuw N, Pfundt R, Koolen DA, Neefs I, Scheltinga I, Mieloo H, Sistermans EA, Nillesen W, Smeets DF, de Vries BB, Knoers NV (2008). "A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis". J Med Genet. 45 (2): 122–4. doi:10.1136/jmg.2007.054049. PMID 18245392. S2CID 972258.
Chabchoub E, Vermeesch JR, de Ravel T, de Cock P, Fryns JP (2008). "The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15". J Med Genet. 45 (3): 189–92. doi:10.1136/jmg.2007.056176. PMID 18310269. S2CID 32961901.
Liang JS, Shimojima K, Ohno K, Sugiura C, Une Y, Ohno K, et al. (2009). "A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion". J Med Genet. 46 (9): 645–7. doi:10.1136/jmg.2008.059220. PMID 19724011. S2CID 5128199.