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Genetics of Head & Neck Disease
Contributing journals to this collection:
JAMA & Archives Journals
Citations 121-130 of 134 total displayed.
- Original Articles
Localization of the Gene for Familial Laryngeal Abductor Paralysis to Chromosome 6q16
- Jose M. Manaligod; Jennifer Skaggs; Richard J. H. Smith
Arch Otolaryngol Head Neck Surg 2001; 127: 913-917.
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- Original Articles
MYO1F as a Candidate Gene for Nonsyndromic Deafness, DFNB15
- Achih H. Chen; Dietrich A. Stephan; Tama Hasson; Kunihiro Fukushima; Christiana M. Nelissen; Arthur F. Chen; Andrew I. Jun; Arabandi Ramesh; Guy Van Camp; Richard J. H. Smith
Arch Otolaryngol Head Neck Surg 2001; 127: 921-925.
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- Original Articles
Connexin 26 Gene Mutations in Congenitally Deaf Children: Pitfalls for Genetic Counseling
- Sandrine Marlin; Éréa-Noël Garabédian; Gilles Roger; Lucien Moatti; Nicole Matha; Patricia Lewin; Christine Petit; Françoise Denoyelle
Arch Otolaryngol Head Neck Surg 2001; 127: 927-933.
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- Original Articles
Pediatric Otolaryngologists' Knowledge and Understanding of Genetic Testing for Deafness
- Nathaniel H. Robin; Christin Dietz; James E. Arnold; Richard J. H. Smith
Arch Otolaryngol Head Neck Surg 2001; 127: 937-940.
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- Clinical Notes
Long-term Audiological Feature in Pendred Syndrome Caused by PDS Mutation
- Satoshi Iwasaki; Shin-ichi Usami; Satoko Abe; Haruo Isoda; Takahiro Watanabe; Tomoyuki Hoshino
Arch Otolaryngol Head Neck Surg 2001; 127: 705-708.
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- Original Articles
Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13)
- Els M. R. De Leenheer; Henricus P. M. Kunst; Wyman T. McGuirt; Sai D. Prasad; Matthew R. Brown; Patrick L. M. Huygen; Richard J. H. Smith; Cor W. R. J. Cremers
Arch Otolaryngol Head Neck Surg 2001; 127: 13-17.
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- Original Articles
Two Distinct Regions of Loss on Chromosome Arm 4q in Primary Head and Neck Squamous Cell Carcinoma
- Shefali I. Shah; Lin Yip; Ben Greenberg; Joseph A. Califano; John Chow; Claus F. Eisenberger; Daniel J. Lee; Duane A. Sewell; Andre L. Reed; Miriam Lango; Jin Jen; Wayne M. Koch; David Sidransky
Arch Otolaryngol Head Neck Surg 2000; 126: 1073-1076.
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- Original Articles
Clinical Characterization of Genetic Hearing Loss Caused by a Mutation in the POU4F3 Transcription Factor
- Moshe Frydman; Sarah Vreugde; Ben I. Nageris; Sigal Weiss; Oz Vahava; Karen B. Avraham
Arch Otolaryngol Head Neck Surg 2000; 126: 633-637.
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- Corrections
Error in Financial Support Acknowledgment
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Arch Otolaryngol Head Neck Surg 1999; 125: 1285.
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- Original Articles
Genetic Associations in Age-Related Hearing Thresholds
- George A. Gates; Nat N. Couropmitree; Richard H. Myers
Arch Otolaryngol Head Neck Surg 1999; 125: 654-659.
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