Deletion 9q34.3 syndrome: Genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly

S. A. Yatsenko, S. W. Cheung, D. A. Scott, M. J.M. Nowaczyk, M. Tarnopolsky, S. Naidu, G. Bibat, A. Patel, J. G. Leroy, F. Scaglia, P. Stankiewicz, James R. Lupski

Research output: Contribution to journalArticle

Original languageEnglish (US)
Pages (from-to)328-335
Number of pages8
JournalJournal of medical genetics
Volume42
Issue number4
DOIs
StatePublished - Apr 2005

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Yatsenko, S. A., Cheung, S. W., Scott, D. A., Nowaczyk, M. J. M., Tarnopolsky, M., Naidu, S., Bibat, G., Patel, A., Leroy, J. G., Scaglia, F., Stankiewicz, P., & Lupski, J. R. (2005). Deletion 9q34.3 syndrome: Genotype-phenotype correlations and an extended deletion in a patient with features of Opitz C trigonocephaly. Journal of medical genetics, 42(4), 328-335. https://doi.org/10.1136/jmg.2004.028258