E-LIB Suche - Ergebnisse für: Santos, Regie Lyn P

1

Localization of a novel autosomal recessive nonsyndromic he..:

Tariq, Aamira ; Santos, Regie Lyn P. ; Khan, Mohammad Nasim...
Journal of Molecular Medicine. 84 (2006) 6 - p. 484-490 , 2006

Link: https://doi.org/10.1007/..

2

DFNB68, a novel autosomal recessive non-syndromic hearing i..:

Santos, Regie Lyn P. ; Hassan, Muhammad Jawad ; Sikandar, Shaheen...
Human Genetics. 120 (2006) 1 - p. 85-92 , 2006

Link: https://doi.org/10.1007/..

3

Hearing impairment in Dutch patients with connexin 26 (GJB2..:

Santos, Regie Lyn P. ; Aulchenko, Yurii S. ; Huygen, Patrick L.M....
International Journal of Pediatric Otorhinolaryngology. 69 (2005) 2 - p. 165-174 , 2005

Link: https://doi.org/10.1016/..

4

Novel sequence variants in the TMIE gene in families with a..:

Santos, Regie Lyn P. ; El-Shanti, Hatem ; Sikandar, Shaheen...
Journal of Molecular Medicine. 84 (2005) 3 - p. 226-231 , 2005

Link: https://doi.org/10.1007/..

5

A novel autosomal recessive non-syndromic hearing impairmen..:

Hassan, Muhammad Jawad ; Santos, Regie Lyn P. ; Rafiq, Muhammad Arshad...
Human Genetics. 118 (2005) 5 - p. 605-610 , 2005

Link: https://doi.org/10.1007/..

6

The A2ml1-Knockout mouse as an animal model for non-syndrom..:

Elling, Christina L. ; Gomez, Helen Z. ; Lee, Nam K...
International Journal of Pediatric Otorhinolaryngology. 181 (2024) - p. 111980 , 2024

Link: https://doi.org/10.1016/..

7

Clinical Genetic Testing for Hearing Loss: Implications for..:

Lee, Nam K. ; Uhler, Kristin M. ; Yoon, Patricia J..
Biomedicines. 12 (2024) 7 - p. 1427 , 2024

Link: https://doi.org/10.3390/..

8

Genetics and Otitis Media:

, In: Textbook of Otitis Media,

Lee, Nam K. ; Santos-Cortez, Regie Lyn P. - p. 91-107 , 2023

Link: https://doi.org/10.1007/..

9

Rare Coding Variants in Patients with Non-Syndromic Vestibu..:

Sumalde, Angelo Augusto M. ; Scholes, Melissa A. ; Kalmanson, Olivia A....
Genes. 14 (2023) 4 - p. 831 , 2023

Link: https://doi.org/10.3390/..

10

Novel candidate genes for cholesteatoma in chronic otitis m..:

Lee, Nam K. ; Cass, Stephen P. ; Gubbels, Samuel P....
Frontiers in Genetics. 13 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

11

A loss of function variant in AGPAT3 underlies intellectual..:

Malik, Madiha Amin ; Saqib, Muhammad Arif Nadeem ; Mientjes, Edwin...
European Journal of Human Genetics. 31 (2023) 12 - p. 1447-1454 , 2023

Link: https://doi.org/10.1038/..

12

Editorial: Otitis media susceptibility due to genetic varia..:

Marom, Tal ; Swords, W. Edward ; Santos-Cortez, Regie Lyn P.
Frontiers in Genetics. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

13

Ensuring the future of otitis media research: Interest in a..:

Ziniel, Sonja I. ; Preciado, Diego ; Lee, Rita...
International Journal of Pediatric Otorhinolaryngology. 172 (2023) - p. 111693 , 2023

Link: https://doi.org/10.1016/..

14

The FUT2 Variant c.461G>A (p.Trp154*) Is Associated With Di..:

Elling, Christina L. ; Scholes, Melissa A. ; Streubel, Sven-Olrik...
Frontiers in Cellular and Infection Microbiology. 11 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

15

Microbiota Associated With Cholesteatoma Tissue in Chronic ..:

Frank, Daniel N. ; Magno, Jose Pedrito M. ; Velasco, Karen Joyce S....
Frontiers in Cellular and Infection Microbiology. 12 (2022) - p. , 2022

Link: https://doi.org/10.3389/..