Recurrent tonsillitis among twinsSMITH, Richard J. H.JAMA, the journal of the American Medical Association. 2005, Vol 293, Num 23, pp 2925-2926, issn 0098-7484, 2 p.Article

Clinical application of genetic testing for deafness : Genetics of deafnessSMITH, Richard J. H.American journal of medical genetics. 2004, Vol 130A, Num 1, pp 8-12, issn 0148-7299, 5 p.Article

Current Treatment Paradigms in the Management of Lymphatic MalformationsRENTON, John P; SMITH, Richard J. H.The Laryngoscope. 2011, Vol 121, Num 1, pp 56-59, issn 0023-852X, 4 p.Article

Monitoring Stress Levels in Postgraduate Medical TrainingHILL, Justin D; SMITH, Richard J. H.The Laryngoscope. 2009, Vol 119, Num 1, pp 75-78, issn 0023-852X, 4 p.Article

The Genetics of otosclerosisEALY, Megan; SMITH, Richard J. H.Hearing research. 2010, Vol 266, Num 1-2, pp 70-74, issn 0378-5955, 5 p.Article

Did the GJB2 35delG Mutation Originate in Iran?NOROUZI, Vahideh; AZIZI, Hiva; NAJMABADI, Hossein et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 10, pp 2453-2458, issn 1552-4825, 6 p.Article

The Prevalence of Mitochondrial Mutations Associated with Aminoglycoside-Induced Sensorineural Hearing Loss in an NICU PopulationEALY, Megan; LYNCH, Katherine A; MEYER, Nicole C et al.The Laryngoscope. 2011, Vol 121, Num 6, pp 1184-1186, issn 0023-852X, 3 p.Article

Polymorphisms in KCNε1 or KCNε3 Are Not Associated With Ménière Disease in the Caucasian PopulationCAMPBELL, Colleen A; DELLA SANTINA, Charley C; GANTZ, Bruce J et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 1, pp 67-74, issn 1552-4825, 8 p.Article

A Novel Mutation in COCH-Implications for Genotype-Phenotype Correlations in DFNA9 Hearing LossHILDEBRAND, Michael S; GANDOLFO, Luke; SHEARER, A. Eliot et al.The Laryngoscope. 2010, Vol 120, Num 12, pp 2489-2493, issn 0023-852X, 5 p.Article

The coding polymorphism T2631 in TGF-β1 is associated with otosclerosis in two independent populationsTHYS, Melissa; SCHRAUWEN, Isabelle; CREMERS, Cor R. W. J et al.Human molecular genetics (Print). 2007, Vol 16, Num 17, pp 2021-2030, issn 0964-6906, 10 p.Article

Membranoproliferative glomerulonephritis type II (dense deposit disease) : An updateAPPEL, Gerald B; COOK, H. Terence; ROSE, Noel R et al.Journal of the American Society of Nephrology. 2005, Vol 16, Num 5, pp 1392-1403, issn 1046-6673, 12 p.Article

Case of progressive dysplasia concomitant with intralesional cidofovir administration for recurrent respiratory papillomatosisWEMER, Richard D; LEE, John H; HOFFMAN, Henry T et al.The Annals of otology, rhinology & laryngology. 2005, Vol 114, Num 11, pp 836-839, issn 0003-4894, 4 p.Article

Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutationsPRASAD, Sai; KÖLLN, Karen A; CUCCI, Robert A et al.American journal of medical genetics. 2004, Vol 124A, Num 1, pp 1-9, issn 0148-7299, 9 p.Article

Searching for evidence of DFNB2ASTUTO, Lisa M; KELLEY, Philip M; ASKEW, James W et al.American journal of medical genetics. 2002, Vol 109, Num 4, pp 291-297, issn 0148-7299Article

Treatment of lymphangiomas with OK-432 (Picibanil) sclerotherapy: A prospective multi-institutional trialGIGUERE, Chantal M; BAUMAN, Nancy M; SATO, Yutaka et al.Archives of otolaryngology, head & neck surgery. 2002, Vol 128, Num 10, pp 1137-1144, issn 0886-4470Article

Localization of the gene for familial laryngeal abductor paralysis to chromosome 6q16MANALIGOD, Jose M; SKAGGS, Jennifer; SMITH, Richard J. H et al.Archives of otolaryngology, head & neck surgery. 2001, Vol 127, Num 8, pp 913-917, issn 0886-4470Article

Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafnessROBIN, Nathaniel H; DIETZ, Christin; ARNOLD, James E et al.Archives of otolaryngology, head & neck surgery. 2001, Vol 127, Num 8, pp 937-940, issn 0886-4470Article

Age-related mitochondrial DNA mutations in the human larynxMANALIGOD, Jose M; MILAM, Michael; HILL, Sarah Ann et al.The Laryngoscope. 2000, Vol 110, Num 12, pp 2123-2127, issn 0023-852XArticle

Deafness in the genomics eraSHEARER, A. Eliot; HILDEBRAND, Michael S; SLOAN, Christina M et al.Hearing research. 2011, Vol 282, Num 1-2, pp 1-9, issn 0378-5955, 9 p.Article

A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with OtosclerosisSCHRAUWEN, Isabelle; EALY, Megan; CREMERS, Cor W. R. J et al.American journal of human genetics. 2009, Vol 84, Num 3, pp 328-338, issn 0002-9297, 11 p.Article

Factor I and factor H deficiency in renal diseases : similar defects in the fluid phase have a different outcome at the surface of the glomerular basement membraneZIPFEL, Peter F; SMITH, Richard J. H; SKERKA, Christine et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 2, pp 385-387, issn 0931-0509, 3 p.Article

Glomeruli of Dense Deposit Disease contain components of the alternative and terminal complement pathwaySETHI, Sanjeev; GAMEZ, Jeffrey D; VRANA, Julie A et al.Kidney international. 2009, Vol 75, Num 9, pp 952-960, issn 0085-2538, 9 p.Article

Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in HumansGRILLET, Nicolas; SCHWANDER, Martin; STEPHAN, Dietrich et al.American journal of human genetics. 2009, Vol 85, Num 3, pp 328-337, issn 0002-9297, 10 p.Article

Mutations of KCNJ10 Together with Mutations of SLC26A4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct SyndromeTAO YANG; GURROLA, Jose G; HAO WU et al.American journal of human genetics. 2009, Vol 84, Num 5, pp 651-657, issn 0002-9297, 7 p.Article

Recurrent Atypical Hemolytic Uremic Syndrome Associated With Factor I Mutation in a Living Related Renal Transplant RecipientCHAN, Micah R; THOMAS, Christie P; TORREALBA, Jose R et al.American journal of kidney diseases. 2009, Vol 53, Num 2, pp 321-326, issn 0272-6386, 6 p.Article