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Hội chứng xa mất đoạn 22q11.2 (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hội chứng xa mất đoạn 22q11.2" in Vietnamese language version.

refsWebsite
Global rank Vietnamese rank
6nih.gov
4th place
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3doi.org
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2nd place
2archive.org
6th place
4th place

archive.org

doi.org

  • Garavelli, L.; Rosato, S.; Wischmeijer, A.; Gelmini, C.; Esposito, A.; Mazzanti, L.; Franchi, F.; De Crescenzo, A.; Palumbo, O.; Carella, M.; Riccio, A. (2011). “22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review”. Mol Syndromol. 2 (1): 35–44. doi:10.1159/000334262. PMC 3343753. PMID 22582037.
  • 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 (tháng 1 năm 2008). “22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome”. Am J Hum Genet. 82 (1): 214–21. doi:10.1016/j.ajhg.2007.09.014. PMC 2253964. PMID 18179902.
  • Saitta, SC; McGrath JM; Mensch H; Shaikh TH; Zackai EH; Emanuel BS Am J Hum Genet (tháng 8 năm 1999). “A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects”. Am J Hum Genet. 65 (2): 562–6. doi:10.1086/302514. PMC 1377955. PMID 10417299.

nih.gov

ncbi.nlm.nih.gov

  • Garavelli, L.; Rosato, S.; Wischmeijer, A.; Gelmini, C.; Esposito, A.; Mazzanti, L.; Franchi, F.; De Crescenzo, A.; Palumbo, O.; Carella, M.; Riccio, A. (2011). “22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review”. Mol Syndromol. 2 (1): 35–44. doi:10.1159/000334262. PMC 3343753. PMID 22582037.
  • 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 (tháng 1 năm 2008). “22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome”. Am J Hum Genet. 82 (1): 214–21. doi:10.1016/j.ajhg.2007.09.014. PMC 2253964. PMID 18179902.
  • Saitta, SC; McGrath JM; Mensch H; Shaikh TH; Zackai EH; Emanuel BS Am J Hum Genet (tháng 8 năm 1999). “A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects”. Am J Hum Genet. 65 (2): 562–6. doi:10.1086/302514. PMC 1377955. PMID 10417299.

pubmed.ncbi.nlm.nih.gov

  • Garavelli, L.; Rosato, S.; Wischmeijer, A.; Gelmini, C.; Esposito, A.; Mazzanti, L.; Franchi, F.; De Crescenzo, A.; Palumbo, O.; Carella, M.; Riccio, A. (2011). “22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review”. Mol Syndromol. 2 (1): 35–44. doi:10.1159/000334262. PMC 3343753. PMID 22582037.
  • 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 (tháng 1 năm 2008). “22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome”. Am J Hum Genet. 82 (1): 214–21. doi:10.1016/j.ajhg.2007.09.014. PMC 2253964. PMID 18179902.
  • Saitta, SC; McGrath JM; Mensch H; Shaikh TH; Zackai EH; Emanuel BS Am J Hum Genet (tháng 8 năm 1999). “A 22q11.2 deletion that excludes UFD1L and CDC45L in a patient with conotruncal and craniofacial defects”. Am J Hum Genet. 65 (2): 562–6. doi:10.1086/302514. PMC 1377955. PMID 10417299.