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Alford, Raye L. [Other]

Medical genetics in the clinical practice of ORL : 20 tables

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Basel; Freiburg [u.a.]: Karger, 2011

Published in: Advances in oto-rhino-laryngology ; 70
Alford, Raye L. [Other]

Medical genetics in the clinical practice of ORL

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Basel; Freiburg [u.a.]: Karger, 2011

Published in: Advances in oto-rhino-laryngology ; 70
Alford, Raye L.

Medical Genetics in the Clinical Practice of ORL: Nonsyndromic Hereditary Hearing Loss

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S. Karger AG, 2011

Published in: Medical Genetics in the Clinical Practice of ORL (2011), Seite 37-42
Fang, Ping; Alford, Raye L.

Medical genetics and genomics curricula focused on the laboratory specialties

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Elsevier BV, 2012

Published in: Genetics in Medicine, 14 (2012) 3, Seite 349
Alford, Raye L.; Darilek, Sandra A.

Medical Genetics in the Clinical Practice of ORL: Basic Medical Genetics for the Otolaryngologist

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S. Karger AG, 2011

Published in: Medical Genetics in the Clinical Practice of ORL (2011), Seite 10-17
Vrabec, Jeffrey T; Alford, Raye L

Quantitative analysis of herpes simplex virus in cranial nerve ganglia

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Springer Science and Business Media LLC, 2004

Published in: Journal of Neurovirology, 10 (2004) 4, Seite 216-222
Alford, Raye L.; Belmont, John W.

Stable RNA Secondary Structure in a Retroviral Vector Insert Terminates Reverse Transcriptase ElongationIn Vitrobut Not in Cultured Cells

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Mary Ann Liebert Inc, 1990

Published in: Human Gene Therapy, 1 (1990) 3, Seite 269-276
Reza, Nosheen; Alford, Raye L.; Belmont, John W.; Marston, Nicholas

The Expansion of Genetic Testing in Cardiovascular Medicine: Preparing the Cardiology Community for the Changing Landscape

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Springer Science and Business Media LLC, 2024

Published in: Current Cardiology Reports, 26 (2024) 3, Seite 135-146
Alford, Raye L.; Demarchi, Jean M.; Richards, C. Sue

Frequency of a DNA polymorphism at position Y231 in the aspartoacylase gene and its impact on DNA-based carrier testing for Canavan disease in the Ashkenazi Jewish population

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Wiley, 1998

Published in: Human Mutation, 11 (1998) S1, Seite S161-S162
Dhar, Shweta U.; Alford, Raye L.; Nelson, Elizabeth A.; Potocki, Lorraine

Enhancing exposure to genetics and genomics through an innovative medical school curriculum

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Elsevier BV, 2012

Published in: Genetics in Medicine, 14 (2012) 1, Seite 163-167
Dhar, Shweta U.; Alford, Raye L.; Nelson, Elizabeth A.; Potocki, Lorraine

Enhancing exposure to genetics and genomics through an innovative medical school curriculum

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Elsevier BV, 2011

Published in: Genetics in Medicine (2011), Seite 1
Tang, Hsiao-Yuan; Xia, Anping; Oghalai, John S; Pereira, Fred A; Alford, Raye L

High frequency of the IVS2-2AG DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss

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Springer Science and Business Media LLC, 2005

Published in: BMC Medical Genetics, 6 (2005) 1
Yang, Thomas P.; Stout, John T.; Konecki, David S.; Patel, Pragna I.; Alford, Raye L.; Caskey, C. Thomas

Spontaneous reversion of novel Lesch-Nyhan mutation byHPRT gene rearrangement

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Springer Science and Business Media LLC, 1988

Published in: Somatic Cell and Molecular Genetics, 14 (1988) 3, Seite 293-303
Alford, Raye L.; Arnos, Kathleen S.; Fox, Michelle; Lin, Jerry W.; Palmer, Christina G.; Pandya, Arti; Rehm, Heidi L.; Robin, Nathaniel H.; Scott, Daryl A.; Yoshinaga-Itano, Christine

American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss

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Elsevier BV, 2014

Published in: Genetics in Medicine, 16 (2014) 4, Seite 347-355
Tang, Hsiao-Yuan; Fang, Ping; Lin, Jerry W; Darilek, Sandra; Osborne, Brooke T; Haymond, Jo Ann; Manolidis, Spiros; Roa, Benjamin B; Oghalai, John S; Alford, Raye L

DNA sequence analysis and genotype–phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy

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BMJ, 2015

Published in: BMJ Open, 5 (2015) 5, Seite e007506
Tang, Hsiao‐Yuan; Basehore, Monica J.; Blakey, Gregory L.; Darilek, Sandra; Oghalai, John S.; Roa, Benjamin B.; Fang, Ping; Alford, Raye Lynn

Infrequency of two deletion mutations at the DFNB1 locus in patients and controls

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Wiley, 2008

Published in: American Journal of Medical Genetics Part A, 146A (2008) 7, Seite 934-936
Riegert-Johnson, Douglas L.; Korf, Bruce R.; Alford, Raye Lynn; Broder, Martin I.; Keats, Bronya J.B.; Ormond, Kelly E.; Pyeritz, Reed E.; Watson, Michael S.

Outline of a medical genetics curriculum for internal medicine residency training programs

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Elsevier BV, 2004

Published in: Genetics in Medicine, 6 (2004) 6, Seite 543-547
Alford, Raye L.; Friedman, Thomas B.; B. Keats, Bronya J.; Kimberling, William J.; Proud, Virginia K.; H. Smith, Richard J.; Arnos, Kathleen S.; Korf, Bruce R.; Rehm, Heidi L.; Toriello, Helga V.

Early childhood hearing loss: Clinical and molecular genetics. An educational slide set of the American College of Medical Genetics

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Elsevier BV, 2003

Published in: Genetics in Medicine, 5 (2003) 4, Seite 338-341
Alford, Raye L.; Morris, Kelley E.; Rives, C Michelle; Scherer, Steven E.; Weinstock, George; Gibbs, Richard A.; Ghonima, Karim; Belcher, Mark; Valdes, Hayden; Sumners, Carolyn; Law, Colin; Reiff, Patricia

Genetic testing, biotechnology, and GMOs: A snapshot of public opinion, 2003 through 2004

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Elsevier BV, 2005

Published in: Genetics in Medicine, 7 (2005) 6, Seite 454-455
Brown, Chester W.; Levy, Moise L.; Flaitz, Catherine M.; Reid, Barbara S.; Manolidis, Spiros; Hebert, Adelaide A.; Bender, Matthew M.; Heilstedt, Heidi A.; Plunkett, Katie S.; Fang, Ping; Roa, Benjamin B.; Chung, Pil; Tang, Hsiao-Yuan; Richard, Gabriele; Alford, Raye L.

A Novel GJB2 (Connexin 26) Mutation, F142L, in a Patient with Unusual Mucocutaneous Findings and Deafness

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Elsevier BV, 2003

Published in: Journal of Investigative Dermatology, 121 (2003) 5, Seite 1221-1223

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