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3q29 microdeletion syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "3q29 microdeletion syndrome" in English language version.

refsWebsite
Global rank English rank
9nih.gov
4th place
4th place
6doi.org
2nd place
2nd place
1archive.today
14th place
14th place
1semanticscholar.org
11th place
8th place
1wiley.com
222nd place
297th place

archive.today

doi.org

  • Willatt L, Cox J, Barber J, et al. (July 2005). "3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome". Am. J. Hum. Genet. 77 (1): 154–60. doi:10.1086/431653. PMC 1226188. PMID 15918153.
  • Koochek M (2006). "Clinical and molecular characterization of a new syndrome: the case of 3q29 microdeletion syndrome". Clin. Genet. 69 (2): 121–3. doi:10.1111/j.1399-0004.2006.00570c.x. S2CID 85261528. Archived from the original on 2013-01-05.
  • Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, McDonald M, Campbell L, Ming JE, Zackai EH, Bejjani BA, Shaffer LG (2008). "Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication". Mol Cytogenet. 1: 8. doi:10.1186/1755-8166-1-8. PMC 2408925. PMID 18471269.
  • Cobb W, Anderson A, Turner C, Hoffman RD, Schonberg S, Levin SW (2010). "1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child". Eur J Med Genet. 53 (6): 415–8. doi:10.1016/j.ejmg.2010.08.009. PMID 20832509.
  • Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST (August 2010). "Microdeletions of 3q29 confer high risk for schizophrenia". Am. J. Hum. Genet. 87 (2): 229–36. doi:10.1016/j.ajhg.2010.07.013. PMC 2917706. PMID 20691406.
  • Rees E, Walters JT, Georgieva L, Isles AR, Chambert KD, Richards AL, Mahoney-Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G (February 2014). "Analysis of copy number variations at 15 schizophrenia-associated loci". Br J Psychiatry. 204 (2): 108–14. doi:10.1192/bjp.bp.113.131052. PMC 3909838. PMID 24311552.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Willatt L, Cox J, Barber J, et al. (July 2005). "3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome". Am. J. Hum. Genet. 77 (1): 154–60. doi:10.1086/431653. PMC 1226188. PMID 15918153.
  • Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, McDonald M, Campbell L, Ming JE, Zackai EH, Bejjani BA, Shaffer LG (2008). "Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication". Mol Cytogenet. 1: 8. doi:10.1186/1755-8166-1-8. PMC 2408925. PMID 18471269.
  • Cobb W, Anderson A, Turner C, Hoffman RD, Schonberg S, Levin SW (2010). "1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child". Eur J Med Genet. 53 (6): 415–8. doi:10.1016/j.ejmg.2010.08.009. PMID 20832509.
  • Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST (August 2010). "Microdeletions of 3q29 confer high risk for schizophrenia". Am. J. Hum. Genet. 87 (2): 229–36. doi:10.1016/j.ajhg.2010.07.013. PMC 2917706. PMID 20691406.
  • Rees E, Walters JT, Georgieva L, Isles AR, Chambert KD, Richards AL, Mahoney-Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G (February 2014). "Analysis of copy number variations at 15 schizophrenia-associated loci". Br J Psychiatry. 204 (2): 108–14. doi:10.1192/bjp.bp.113.131052. PMC 3909838. PMID 24311552.

ncbi.nlm.nih.gov

  • Willatt L, Cox J, Barber J, et al. (July 2005). "3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome". Am. J. Hum. Genet. 77 (1): 154–60. doi:10.1086/431653. PMC 1226188. PMID 15918153.
  • Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, McDonald M, Campbell L, Ming JE, Zackai EH, Bejjani BA, Shaffer LG (2008). "Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication". Mol Cytogenet. 1: 8. doi:10.1186/1755-8166-1-8. PMC 2408925. PMID 18471269.
  • Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST (August 2010). "Microdeletions of 3q29 confer high risk for schizophrenia". Am. J. Hum. Genet. 87 (2): 229–36. doi:10.1016/j.ajhg.2010.07.013. PMC 2917706. PMID 20691406.
  • Rees E, Walters JT, Georgieva L, Isles AR, Chambert KD, Richards AL, Mahoney-Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G (February 2014). "Analysis of copy number variations at 15 schizophrenia-associated loci". Br J Psychiatry. 204 (2): 108–14. doi:10.1192/bjp.bp.113.131052. PMC 3909838. PMID 24311552.

semanticscholar.org

api.semanticscholar.org

wiley.com

www3.interscience.wiley.com