22q11.2 distal deletion syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "22q11.2 distal deletion syndrome" in English language version.

refsWebsite

Global rank English rank

9nih.gov

4^th place

5doi.org

2^nd place

1orpha.net

3,537^th place

7,177^th place

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 (Jan 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 (August 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.
Fagberg, CR; Graakjaer J; Heinl UD; Ousager LB; Dreyer I; Kirchhoff M; Rasmussen AA; Lautrup CK; Birkebaek N; Sorensen K. (February 2013). "Heart defects and other features of the 22q11 distal deletion syndrome". Eur J Med Genet. 56 (2): 98–107. doi:10.1016/j.ejmg.2012.09.009. PMID 23063575.
Satoh, Y; Endo S; Nakata T; Kobayashi Y; Yamada K; Ikeda T; Takeuchi A; Hiramoto T; Watanabe Y; Kazama T (Aug 2011). "ERK2 contributes to the control of social behaviors in mice". J Neurosci. 31 (33): 11953–67. doi:10.1523/JNEUROSCI.2349-11.2011. PMC 6623182. PMID 21849556.

nih.gov

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 (Jan 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 (August 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.
Fagberg, CR; Graakjaer J; Heinl UD; Ousager LB; Dreyer I; Kirchhoff M; Rasmussen AA; Lautrup CK; Birkebaek N; Sorensen K. (February 2013). "Heart defects and other features of the 22q11 distal deletion syndrome". Eur J Med Genet. 56 (2): 98–107. doi:10.1016/j.ejmg.2012.09.009. PMID 23063575.
Satoh, Y; Endo S; Nakata T; Kobayashi Y; Yamada K; Ikeda T; Takeuchi A; Hiramoto T; Watanabe Y; Kazama T (Aug 2011). "ERK2 contributes to the control of social behaviors in mice". J Neurosci. 31 (33): 11953–67. doi:10.1523/JNEUROSCI.2349-11.2011. PMC 6623182. PMID 21849556.

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 (Jan 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 (August 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.
Satoh, Y; Endo S; Nakata T; Kobayashi Y; Yamada K; Ikeda T; Takeuchi A; Hiramoto T; Watanabe Y; Kazama T (Aug 2011). "ERK2 contributes to the control of social behaviors in mice". J Neurosci. 31 (33): 11953–67. doi:10.1523/JNEUROSCI.2349-11.2011. PMC 6623182. PMID 21849556.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Distal 22q11.2 microdeletion syndrome". www.orpha.net. Retrieved 26 October 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)