Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

Fulltext present in this item

Fulltext: 22078___.PDF

Format: PDF

Description: publisher's version

Title:	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3
Author(s):	Bitner-Glindzicz, M.; Turnpenny, P.; Höglund, P.; Kääriäinen, H.; Sankila, E.M.; Maarel, S.M. van der; Kok, Y.J.M. de; Ropers, H.-H.; Cremers, F.P.M. ; Pembrey, M.; Malcolm, S.
Publication year:	1995
Source:	Human Molecular Genetics, vol. 4, iss. 8, (1995), pp. 1467-1469
ISSN:	0964-6906
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/22078
Display more details
Organization:	Human Genetics
Journal title:	Human Molecular Genetics
Volume:	vol. 4
Issue:	iss. 8
Page start:	p. 1467
Page end:	p. 1469
Languages used:	en

Academic publications [168098]
Academic output Radboud University
Open Access publications [49210]
Freely accessible full text publications
Electronic publications [76722]
Freely accessible full text publications plus those not yet available due to embargo
Faculty of Medical Sciences [66554]