Suchergebnisse - "Kenna, Margaret A."

PubPharm (174)

1

PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss

enthalten in: Human genetics | 2024

von Redfield, S. | De-la-Torre, P. | Zamani, M. | +14

UpdateOf: medRxiv. 2023 Dec 19;:. - PMID 37873491

2

PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss

enthalten in: Human genetics | 2024

von Redfield, S. | De-la-Torre, P. | Zamani, M. | +14

3

PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss

enthalten in: bioRxiv.org | 2023

von Redfield, S. | De-la-Torre, P. | Zamani, M. | +14

4

PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss

enthalten in: medRxiv : the preprint server for health sciences | 2023

von Redfield, S. | De-la-Torre, P. | Zamani, M. | +14

UpdateIn: Hum Genet. 2024 Mar 9;:. - PMID 38459354

5

Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients

enthalten in: The Laryngoscope | 2023

von Benson, J. | Stewart, C. | Kenna, M. | +1

6

Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients With Enlarged Vestibular Aqueduct or GJB2 Mutation

enthalten in: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology | 2023

von Jahn, K. | Morse-Fortier, C. | Griffin, A. | +5

7

Otolaryngologic Manifestations of Trisomy 13 and Trisomy 18 in Pediatric Patients

enthalten in: The Laryngoscope | 2023

von Benson, J. | Stewart, C. | Kenna, M. | +1

8

Genetic testing for pediatric hearing loss : no time to waste

enthalten in: Human genetics | 2022

von Kenna, M.

9

Evaluation of copy number variants for genetic hearing loss : a review of current approaches and recent findings

enthalten in: Human genetics | 2022

von Abbasi, W. | French, C. | Rockowitz, S. | +2

10

Hearing Aid Use in Children With Unilateral Hearing Loss : A Randomized Crossover Clinical Trial

enthalten in: The Laryngoscope | 2022

von Benchetrit, L. | Stenerson, M. | Ronner, E. | +7

1
2
3
4
5
6
7
8
9
10
11
Nächster »
[18]