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branchio-oculo-facial syndrome, cleft lip/palate, mutation analysis, neurocristopathy, TFAP2A, CHARGE SYNDROME, INTERSTITIAL DELETION, MOLECULAR ANALYSES, INNER-EAR, PATIENT, AP-2

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Citation

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Chicago
Milunsky, Jeff M, Tom M Maher, Geping P Zhao, Zhenyuan Wang, John B Mulliken, David Chitayat, Michele Clemens, et al. 2011. “Genotype-phenotype Analysis of the Branchio-oculo-facial Syndrome.” American Journal of Medical Genetics Part A 155A (1): 22–32.
APA
Milunsky, J. M., Maher, T. M., Zhao, G. P., Wang, Z., Mulliken, J. B., Chitayat, D., Clemens, M., et al. (2011). Genotype-phenotype analysis of the branchio-oculo-facial syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 155A(1), 22–32.
Vancouver
1.
Milunsky JM, Maher TM, Zhao GP, Wang Z, Mulliken JB, Chitayat D, et al. Genotype-phenotype analysis of the branchio-oculo-facial syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2011;155A(1):22–32.
MLA
Milunsky, Jeff M, Tom M Maher, Geping P Zhao, et al. “Genotype-phenotype Analysis of the Branchio-oculo-facial Syndrome.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 155A.1 (2011): 22–32. Print.
@article{1164795,
  author       = {Milunsky, Jeff M and Maher, Tom M and Zhao, Geping P and Wang, Zhenyuan and Mulliken, John B and Chitayat, David and Clemens, Michele and Stalker, Heather J and Bauer, Mislen and Burch, Michele and Chenier, S{\'e}bastien and Cunningham, Michael L and Drack, Arlene V and Janssens, Sandra and Karlea, Audrey and Klatt, Regan and Kini, Usha and Klein, Ophir and Lachmeijer, Augusta M and Megarbane, Andre and Mendelsohn, Nancy J and Meschino, Wendy S and Mortier, Geert and Parkash, Sandhya and Ray, Cenai R and Roberts, Angharad and Roberts, Amy and Reardon, Willie and Schnur, Rhonda E and Smith, Rosemarie and Splitt, Miranda and Tezcan, Kamer and Whiteford, Margo L and Wong, Derek A and Zori, Roberto and Lin, Angela E},
  issn         = {1552-4825},
  journal      = {AMERICAN JOURNAL OF MEDICAL GENETICS PART A},
  keyword      = {branchio-oculo-facial syndrome,cleft lip/palate,mutation analysis,neurocristopathy,TFAP2A,CHARGE SYNDROME,INTERSTITIAL DELETION,MOLECULAR ANALYSES,INNER-EAR,PATIENT,AP-2},
  language     = {eng},
  number       = {1},
  pages        = {22--32},
  title        = {Genotype-phenotype analysis of the branchio-oculo-facial syndrome},
  url          = {http://dx.doi.org/10.1002/ajmg.a.33783},
  volume       = {155A},
  year         = {2011},
}

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