Brachydactyly (English Wikipedia)

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

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clevelandclinic.org

my.clevelandclinic.org

doi.org

  • Pierpont, Mary Ella; Brueckner, Martina; Chung, Wendy K.; Garg, Vidu; Lacro, Ronald V.; McGuire, Amy L.; Mital, Seema; Priest, James R.; Pu, William T.; Roberts, Amy; Ware, Stephanie M.; Gelb, Bruce D.; Russell, Mark W. (2018-11-20). "Genetic Basis for Congenital Heart Disease: Revisited". Circulation. 138 (21): e653–e711. doi:10.1161/CIR.0000000000000606. ISSN 0009-7322. PMC 6555769. PMID 30571578.
  • Jenkins, Dagan; Seelow, Dominik; Jehee, Fernanda S.; Perlyn, Chad A.; Alonso, Luís G.; Bueno, Daniela F.; Donnai, Dian; Josifiova, Dragana; Mathijssen, Irene M. J.; Morton, Jenny E. V.; Helene Ørstavik, Karen; Sweeney, Elizabeth; Wall, Steven A.; Marsh, Jeffrey L.; Nürnberg, Peter (2007-06-01). "RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity". The American Journal of Human Genetics. 80 (6): 1162–1170. doi:10.1086/518047. ISSN 0002-9297. PMC 1867103. PMID 17503333.
  • Wlodarczyk, Bogdan J.; Palacios, Ana M.; George, Timothy M.; Finnell, Richard H. (2012). "Antiepileptic drugs and pregnancy outcomes". American Journal of Medical Genetics Part A. 158A (8): 2071–2090. doi:10.1002/ajmg.a.35438. PMC 3402584. PMID 22711424.
  • Temtamy, Samia A.; Aglan, Mona S. (2008-06-13). "Brachydactyly". Orphanet Journal of Rare Diseases. 3 (1): 15. doi:10.1186/1750-1172-3-15. ISSN 1750-1172. PMC 2441618. PMID 18554391.
  • Meiselman SA, Berkenstadt M, Ben-Ami T, Goodman RM (1989). "Brachydactyly type A-7 (Smorgasbord): a new entity". Clin. Genet. 35 (4): 261–7. doi:10.1111/j.1399-0004.1989.tb02940.x. PMID 2714013. S2CID 30099363.

genome.gov

medscape.com

emedicine.medscape.com

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Pierpont, Mary Ella; Brueckner, Martina; Chung, Wendy K.; Garg, Vidu; Lacro, Ronald V.; McGuire, Amy L.; Mital, Seema; Priest, James R.; Pu, William T.; Roberts, Amy; Ware, Stephanie M.; Gelb, Bruce D.; Russell, Mark W. (2018-11-20). "Genetic Basis for Congenital Heart Disease: Revisited". Circulation. 138 (21): e653–e711. doi:10.1161/CIR.0000000000000606. ISSN 0009-7322. PMC 6555769. PMID 30571578.
  • Jenkins, Dagan; Seelow, Dominik; Jehee, Fernanda S.; Perlyn, Chad A.; Alonso, Luís G.; Bueno, Daniela F.; Donnai, Dian; Josifiova, Dragana; Mathijssen, Irene M. J.; Morton, Jenny E. V.; Helene Ørstavik, Karen; Sweeney, Elizabeth; Wall, Steven A.; Marsh, Jeffrey L.; Nürnberg, Peter (2007-06-01). "RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity". The American Journal of Human Genetics. 80 (6): 1162–1170. doi:10.1086/518047. ISSN 0002-9297. PMC 1867103. PMID 17503333.
  • Wlodarczyk, Bogdan J.; Palacios, Ana M.; George, Timothy M.; Finnell, Richard H. (2012). "Antiepileptic drugs and pregnancy outcomes". American Journal of Medical Genetics Part A. 158A (8): 2071–2090. doi:10.1002/ajmg.a.35438. PMC 3402584. PMID 22711424.
  • Temtamy, Samia A.; Aglan, Mona S. (2008-06-13). "Brachydactyly". Orphanet Journal of Rare Diseases. 3 (1): 15. doi:10.1186/1750-1172-3-15. ISSN 1750-1172. PMC 2441618. PMID 18554391.
  • Temtamy, Samia (1978). ""The genetics of hand malformations."". Birth Defects Original Article Series. 14 (3): i–xviii, 1–619. PMID 215242.
  • Meiselman SA, Berkenstadt M, Ben-Ami T, Goodman RM (1989). "Brachydactyly type A-7 (Smorgasbord): a new entity". Clin. Genet. 35 (4): 261–7. doi:10.1111/j.1399-0004.1989.tb02940.x. PMID 2714013. S2CID 30099363.

ncbi.nlm.nih.gov

  • Pierpont, Mary Ella; Brueckner, Martina; Chung, Wendy K.; Garg, Vidu; Lacro, Ronald V.; McGuire, Amy L.; Mital, Seema; Priest, James R.; Pu, William T.; Roberts, Amy; Ware, Stephanie M.; Gelb, Bruce D.; Russell, Mark W. (2018-11-20). "Genetic Basis for Congenital Heart Disease: Revisited". Circulation. 138 (21): e653–e711. doi:10.1161/CIR.0000000000000606. ISSN 0009-7322. PMC 6555769. PMID 30571578.
  • Jenkins, Dagan; Seelow, Dominik; Jehee, Fernanda S.; Perlyn, Chad A.; Alonso, Luís G.; Bueno, Daniela F.; Donnai, Dian; Josifiova, Dragana; Mathijssen, Irene M. J.; Morton, Jenny E. V.; Helene Ørstavik, Karen; Sweeney, Elizabeth; Wall, Steven A.; Marsh, Jeffrey L.; Nürnberg, Peter (2007-06-01). "RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity". The American Journal of Human Genetics. 80 (6): 1162–1170. doi:10.1086/518047. ISSN 0002-9297. PMC 1867103. PMID 17503333.
  • Wlodarczyk, Bogdan J.; Palacios, Ana M.; George, Timothy M.; Finnell, Richard H. (2012). "Antiepileptic drugs and pregnancy outcomes". American Journal of Medical Genetics Part A. 158A (8): 2071–2090. doi:10.1002/ajmg.a.35438. PMC 3402584. PMID 22711424.
  • Temtamy, Samia A.; Aglan, Mona S. (2008-06-13). "Brachydactyly". Orphanet Journal of Rare Diseases. 3 (1): 15. doi:10.1186/1750-1172-3-15. ISSN 1750-1172. PMC 2441618. PMID 18554391.

semanticscholar.org

api.semanticscholar.org

webmd.com

worldcat.org

  • Pierpont, Mary Ella; Brueckner, Martina; Chung, Wendy K.; Garg, Vidu; Lacro, Ronald V.; McGuire, Amy L.; Mital, Seema; Priest, James R.; Pu, William T.; Roberts, Amy; Ware, Stephanie M.; Gelb, Bruce D.; Russell, Mark W. (2018-11-20). "Genetic Basis for Congenital Heart Disease: Revisited". Circulation. 138 (21): e653–e711. doi:10.1161/CIR.0000000000000606. ISSN 0009-7322. PMC 6555769. PMID 30571578.
  • Jenkins, Dagan; Seelow, Dominik; Jehee, Fernanda S.; Perlyn, Chad A.; Alonso, Luís G.; Bueno, Daniela F.; Donnai, Dian; Josifiova, Dragana; Mathijssen, Irene M. J.; Morton, Jenny E. V.; Helene Ørstavik, Karen; Sweeney, Elizabeth; Wall, Steven A.; Marsh, Jeffrey L.; Nürnberg, Peter (2007-06-01). "RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity". The American Journal of Human Genetics. 80 (6): 1162–1170. doi:10.1086/518047. ISSN 0002-9297. PMC 1867103. PMID 17503333.
  • Temtamy, Samia A.; Aglan, Mona S. (2008-06-13). "Brachydactyly". Orphanet Journal of Rare Diseases. 3 (1): 15. doi:10.1186/1750-1172-3-15. ISSN 1750-1172. PMC 2441618. PMID 18554391.
  • Idengaku Zasshi, Jinrui (1962) [March 1962]. "The Japanese journal of human genetics". The Japanese Journal of Human Genetics. 7: 10–9. ISSN 0021-5074.