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Elisabeth H Hoefsloot

Showing results (1-10 of 5) with videos related to

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The Journal of Investigative Dermatology|July 13, 2004
A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutationMaurice A M van Steensel, Peter M Steijlen, Reno S Bladergroen, et al.
Orphanet Journal of Rare Diseases|September 19, 2015
Meier-Gorlin syndromeSonja A de Munnik, Elisabeth H Hoefsloot, Jolt Roukema, et al.
Molecular Vision|January 14, 2010
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1Barend F T Hogewind, Ronald J E Pennings, Frans A Hol, et al.
Retina (Philadelphia, Pa.)|April 10, 2009
Clinical and molecular genetic analysis of best vitelliform macular dystrophyCamiel J F Boon, Thomas Theelen, Elisabeth H Hoefsloot, et al.
Ear and Hearing|September 3, 2015
Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing ImpairmentEline van Beelen, Anne M M Oonk, Joop M Leijendeckers, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
The Journal of Investigative Dermatology|July 13, 2004
A phenotype resembling the Clouston syndrome with deafness is associated with a novel missense GJB2 mutationMaurice A M van Steensel, Peter M Steijlen, Reno S Bladergroen, et al.
Orphanet Journal of Rare Diseases|September 19, 2015
Meier-Gorlin syndromeSonja A de Munnik, Elisabeth H Hoefsloot, Jolt Roukema, et al.
Molecular Vision|January 14, 2010
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1Barend F T Hogewind, Ronald J E Pennings, Frans A Hol, et al.
Retina (Philadelphia, Pa.)|April 10, 2009
Clinical and molecular genetic analysis of best vitelliform macular dystrophyCamiel J F Boon, Thomas Theelen, Elisabeth H Hoefsloot, et al.
Ear and Hearing|September 3, 2015
Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing ImpairmentEline van Beelen, Anne M M Oonk, Joop M Leijendeckers, et al.
Pageof 1