A submicroscopic deletion in a patient with isola ted X-linked ocular albinism (OA1)

Maria T. Bassi, Arthur A B Bergen, Martin C. Wapenaar, Maria V. Schiaffino, Mary Van Schooneveld, John R W Yates, Stephen J. Charles, Thomas Meitinger, Andrea Ballabio

Research output: Contribution to journalArticle

11 Citations (Scopus)
Original languageEnglish
Pages (from-to)647-648
Number of pages2
JournalHuman Molecular Genetics
Volume3
Issue number4
Publication statusPublished - Apr 1994

ASJC Scopus subject areas

  • Genetics
  • Statistics, Probability and Uncertainty
  • Applied Mathematics
  • Public Health, Environmental and Occupational Health
  • Molecular Biology
  • Genetics(clinical)

Cite this

Bassi, M. T., Bergen, A. A. B., Wapenaar, M. C., Schiaffino, M. V., Van Schooneveld, M., Yates, J. R. W., ... Ballabio, A. (1994). A submicroscopic deletion in a patient with isola ted X-linked ocular albinism (OA1). Human Molecular Genetics, 3(4), 647-648.

A submicroscopic deletion in a patient with isola ted X-linked ocular albinism (OA1). / Bassi, Maria T.; Bergen, Arthur A B; Wapenaar, Martin C.; Schiaffino, Maria V.; Van Schooneveld, Mary; Yates, John R W; Charles, Stephen J.; Meitinger, Thomas; Ballabio, Andrea.

In: Human Molecular Genetics, Vol. 3, No. 4, 04.1994, p. 647-648.

Research output: Contribution to journalArticle

Bassi, MT, Bergen, AAB, Wapenaar, MC, Schiaffino, MV, Van Schooneveld, M, Yates, JRW, Charles, SJ, Meitinger, T & Ballabio, A 1994, 'A submicroscopic deletion in a patient with isola ted X-linked ocular albinism (OA1)', Human Molecular Genetics, vol. 3, no. 4, pp. 647-648.
Bassi MT, Bergen AAB, Wapenaar MC, Schiaffino MV, Van Schooneveld M, Yates JRW et al. A submicroscopic deletion in a patient with isola ted X-linked ocular albinism (OA1). Human Molecular Genetics. 1994 Apr;3(4):647-648.
Bassi, Maria T. ; Bergen, Arthur A B ; Wapenaar, Martin C. ; Schiaffino, Maria V. ; Van Schooneveld, Mary ; Yates, John R W ; Charles, Stephen J. ; Meitinger, Thomas ; Ballabio, Andrea. / A submicroscopic deletion in a patient with isola ted X-linked ocular albinism (OA1). In: Human Molecular Genetics. 1994 ; Vol. 3, No. 4. pp. 647-648.
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