VACTERL association (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "VACTERL association" in English language version.

refsWebsite

Global rank English rank

13nih.gov

4^th place

8doi.org

2^nd place

1worldcat.org

5^th place

1aappublications.org

3,763^rd place

3,602^nd place

1semanticscholar.org

11^th place

8^th place

aappublications.org

pediatrics.aappublications.org

Khoury, MJ; Cordero, JF; Greenberg, F; James, LM; Erickson, JD (May 1983). "A population study of the VACTERL association: evidence for its etiologic heterogeneity". Pediatrics. 71 (5): 815–20. doi:10.1542/peds.71.5.815. PMID 6835768. S2CID 245102571.

doi.org

Hersh JH, Angle B, Fox TL, Barth RF, Bendon RW, Gowans G (2002). "Developmental field defects: coming together of associations and sequences during blastogenesis". Am J Med Genet. 110 (4): 320–3. doi:10.1002/ajmg.10429. PMID 12116204.
Shaw-Smith, C (July 2006). "Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology". Journal of Medical Genetics. 43 (7): 545–54. doi:10.1136/jmg.2005.038158. PMC 2564549. PMID 16299066.
Rittler, M; Paz, JE; Castilla, EE (Jun 28, 1996). "VACTERL association, epidemiologic definition and delineation". American Journal of Medical Genetics. 63 (4): 529–36. doi:10.1002/(sici)1096-8628(19960628)63:4<529::aid-ajmg4>3.0.co;2-j. PMID 8826430.
Solomon, BD (Aug 16, 2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6: 56. doi:10.1186/1750-1172-6-56. PMC 3169446. PMID 21846383.
Solomon, Benjamin D (2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6 (1): 56. doi:10.1186/1750-1172-6-56. ISSN 1750-1172. PMC 3169446. PMID 21846383.
Khoury, MJ; Cordero, JF; Greenberg, F; James, LM; Erickson, JD (May 1983). "A population study of the VACTERL association: evidence for its etiologic heterogeneity". Pediatrics. 71 (5): 815–20. doi:10.1542/peds.71.5.815. PMID 6835768. S2CID 245102571.
Corsello, G; Giuffrè, L (Jan 1, 1994). "VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance". American Journal of Medical Genetics. 49 (1): 137–8. doi:10.1002/ajmg.1320490133. PMID 8172244.
Placa, Simona; Mario, Gluffre (2013). "Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?". Italian Journal of Pediatrics. 39 (1): 1–8. doi:10.1186/1824-7288-39-45. PMC 3726359. PMID 23842449.

nih.gov

pubmed.ncbi.nlm.nih.gov

Hersh JH, Angle B, Fox TL, Barth RF, Bendon RW, Gowans G (2002). "Developmental field defects: coming together of associations and sequences during blastogenesis". Am J Med Genet. 110 (4): 320–3. doi:10.1002/ajmg.10429. PMID 12116204.
Shaw-Smith, C (July 2006). "Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology". Journal of Medical Genetics. 43 (7): 545–54. doi:10.1136/jmg.2005.038158. PMC 2564549. PMID 16299066.
Rittler, M; Paz, JE; Castilla, EE (Jun 28, 1996). "VACTERL association, epidemiologic definition and delineation". American Journal of Medical Genetics. 63 (4): 529–36. doi:10.1002/(sici)1096-8628(19960628)63:4<529::aid-ajmg4>3.0.co;2-j. PMID 8826430.
Solomon, BD (Aug 16, 2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6: 56. doi:10.1186/1750-1172-6-56. PMC 3169446. PMID 21846383.
Solomon, Benjamin D (2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6 (1): 56. doi:10.1186/1750-1172-6-56. ISSN 1750-1172. PMC 3169446. PMID 21846383.
Khoury, MJ; Cordero, JF; Greenberg, F; James, LM; Erickson, JD (May 1983). "A population study of the VACTERL association: evidence for its etiologic heterogeneity". Pediatrics. 71 (5): 815–20. doi:10.1542/peds.71.5.815. PMID 6835768. S2CID 245102571.
Corsello, G; Giuffrè, L (Jan 1, 1994). "VACTERL with hydrocephalus: a further case with probable autosomal recessive inheritance". American Journal of Medical Genetics. 49 (1): 137–8. doi:10.1002/ajmg.1320490133. PMID 8172244.
Placa, Simona; Mario, Gluffre (2013). "Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?". Italian Journal of Pediatrics. 39 (1): 1–8. doi:10.1186/1824-7288-39-45. PMC 3726359. PMID 23842449.

ncbi.nlm.nih.gov

Shaw-Smith, C (July 2006). "Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology". Journal of Medical Genetics. 43 (7): 545–54. doi:10.1136/jmg.2005.038158. PMC 2564549. PMID 16299066.
Solomon, BD (Aug 16, 2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6: 56. doi:10.1186/1750-1172-6-56. PMC 3169446. PMID 21846383.
Solomon, Benjamin D (2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6 (1): 56. doi:10.1186/1750-1172-6-56. ISSN 1750-1172. PMC 3169446. PMID 21846383.
Placa, Simona; Mario, Gluffre (2013). "Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?". Italian Journal of Pediatrics. 39 (1): 1–8. doi:10.1186/1824-7288-39-45. PMC 3726359. PMID 23842449.

ghr.nlm.nih.gov

"VACTERL association". Genetics Home Reference. Retrieved 29 October 2012.

semanticscholar.org

api.semanticscholar.org

Khoury, MJ; Cordero, JF; Greenberg, F; James, LM; Erickson, JD (May 1983). "A population study of the VACTERL association: evidence for its etiologic heterogeneity". Pediatrics. 71 (5): 815–20. doi:10.1542/peds.71.5.815. PMID 6835768. S2CID 245102571.

worldcat.org

search.worldcat.org

Solomon, Benjamin D (2011). "VACTERL/VATER Association". Orphanet Journal of Rare Diseases. 6 (1): 56. doi:10.1186/1750-1172-6-56. ISSN 1750-1172. PMC 3169446. PMID 21846383.