Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction

J. Foster, S. Kapoor, O. Diaz-Horta, A. Singh, C. Abad, A. Rastogi, R. Moharana, O. Tekeli, Katherina Walz, Mustafa Tekin

Research output: Contribution to journalArticle

4 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)589-591
Number of pages3
JournalClinical Genetics
Volume86
Issue number6
DOIs
StatePublished - Dec 1 2014

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Medicine(all)

Cite this

Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. / Foster, J.; Kapoor, S.; Diaz-Horta, O.; Singh, A.; Abad, C.; Rastogi, A.; Moharana, R.; Tekeli, O.; Walz, Katherina; Tekin, Mustafa.

In: Clinical Genetics, Vol. 86, No. 6, 01.12.2014, p. 589-591.

Research output: Contribution to journalArticle

Foster, J, Kapoor, S, Diaz-Horta, O, Singh, A, Abad, C, Rastogi, A, Moharana, R, Tekeli, O, Walz, K & Tekin, M 2014, 'Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction', Clinical Genetics, vol. 86, no. 6, pp. 589-591. https://doi.org/10.1111/cge.12321
Foster J, Kapoor S, Diaz-Horta O, Singh A, Abad C, Rastogi A et al. Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. Clinical Genetics. 2014 Dec 1;86(6):589-591. https://doi.org/10.1111/cge.12321
Foster, J. ; Kapoor, S. ; Diaz-Horta, O. ; Singh, A. ; Abad, C. ; Rastogi, A. ; Moharana, R. ; Tekeli, O. ; Walz, Katherina ; Tekin, Mustafa. / Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction. In: Clinical Genetics. 2014 ; Vol. 86, No. 6. pp. 589-591.
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