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Waardenburg syndrome

Journal of medical genetics, 1997-08, Vol.34 (8), p.656-665

1997

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Noise levels within the ear and post-nasal space in neonates in intensive care

Archives of disease in childhood. Fetal and neonatal edition, 2003-07, Vol.88 (4), p.F315-318

2003

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The mutational spectrum in Waardenburg syndrome

Human molecular genetics, 1995-11, Vol.4 (11), p.2131-2137

1995

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PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

Human molecular genetics, 1994-07, Vol.3 (7), p.1069-1074

1994

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Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

Nature genetics, 1994-11, Vol.8 (3), p.251-255

1994

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Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings

International journal of pediatric otorhinolaryngology, 1999-10, Vol.50 (1), p.3-13

1999

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Waardenburg syndrome type II: Phenotypic findings and diagnostic criteria

American journal of medical genetics, 1995-01, Vol.55 (1), p.95-100

1995

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Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

Nature (London), 1992-02, Vol.355 (6361), p.635-636

1992

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Linkage Studies of Non-Syndromic Recessive Deafness (NSRD) in a Family Originating from the Mirpur Region of Pakistan Maps DFNB1 Centromeric to D13S175

Human molecular genetics, 1996-01, Vol.5 (1), p.169-173

1996

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Hearing aids versus ventilation tubes in persistent otitis media with effusion: a survey of clinical practice

Journal of laryngology and otology, 2001-04, Vol.115 (4), p.274-279

2001

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Otoacoustic emissions in 28 young adults exposed to amplified music

British Journal of Audiology, 1999-08, Vol.33 (4), p.211-222

1999

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Symptomatic congenital cytomegalovirus infection after maternal recurrent infection

The Pediatric infectious disease journal, 1994-01, Vol.13 (1), p.61-63

1994

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Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

Nature genetics, 1993-01, Vol.3 (1), p.26-30

1993

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A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. II. Audiological findings in 93 patients with unilateral vestibular schwannomas

Journal of laryngology and otology, 1996-12, Vol.110 (12), p.1120-1128

1996

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Distortion product emissions in normal-hearing and low-frequency hearing loss carriers of genes for Waardenburg's syndrome

Annals of otology, rhinology & laryngology, 1997-03, Vol.106 (3), p.220-225

1997

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Evaluation of the use of a questionnaire to detect hearing loss in babies in China

International journal of pediatric otorhinolaryngology, 1999-05, Vol.48 (2), p.125-129

1999

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Sensorineural hearing loss and the Marinesco-Sjögren syndrome

Journal of laryngology and otology, 1991-03, Vol.105 (3), p.210-212

Newton, V. E.

1991

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A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. I. Clinical features of neurofibromatosis in patients with unilateral vestibular schwannomas

Journal of laryngology and otology, 1996-07, Vol.110 (7), p.634-640

1996

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Prescription of hearing aids for the elderly: The views of general practitioners

Journal of laryngology and otology, 1992-11, Vol.106 (11), p.963-966

1992

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Waardenburg syndrome type 2 caused by mutations in the human microphthalmia ( MITF ) gene

Nature genetics, 1994-11, Vol.8 (3), p.251-255

1994

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Genetic counselling for isolated hearing loss

Journal of laryngology and otology, 1989-01, Vol.103 (1), p.12-15

Newton, V. E.

1989

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Evaluation of the use of a questionnaire to detect hearing loss in Kenyan pre-school children

International journal of pediatric otorhinolaryngology, 2001-03, Vol.57 (3), p.229-234

2001

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A clinical, genetic and audiological study of patients and families with bilateral acoustic neurofibromatosis

Journal of laryngology and otology, 1993-01, Vol.107 (1), p.6-11

1993

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Sound Localisation in Children with a Severe Unilateral Hearing Loss

Audiology, 1983, Vol.22 (2), p.189-198

Newton, V. E.

1983

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Progressive sensorineural hearing loss in childhood

British Journal of Audiology, 1988, Vol.22 (4), p.287-295

1988

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Waardenburg syndrome

Noise levels within the ear and post-nasal space in neonates in intensive care

The mutational spectrum in Waardenburg syndrome

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings

Waardenburg syndrome type II: Phenotypic findings and diagnostic criteria

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

Linkage Studies of Non-Syndromic Recessive Deafness (NSRD) in a Family Originating from the Mirpur Region of Pakistan Maps DFNB1 Centromeric to D13S175

Hearing aids versus ventilation tubes in persistent otitis media with effusion: a survey of clinical practice

Otoacoustic emissions in 28 young adults exposed to amplified music

Symptomatic congenital cytomegalovirus infection after maternal recurrent infection

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. II. Audiological findings in 93 patients with unilateral vestibular schwannomas

Distortion product emissions in normal-hearing and low-frequency hearing loss carriers of genes for Waardenburg's syndrome

Evaluation of the use of a questionnaire to detect hearing loss in babies in China

Sensorineural hearing loss and the Marinesco-Sjögren syndrome

A clinical, genetic and audiological study of patients and families with unilateral vestibular schwannomas. I. Clinical features of neurofibromatosis in patients with unilateral vestibular schwannomas

Prescription of hearing aids for the elderly: The views of general practitioners

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia ( MITF ) gene

Genetic counselling for isolated hearing loss

Evaluation of the use of a questionnaire to detect hearing loss in Kenyan pre-school children

A clinical, genetic and audiological study of patients and families with bilateral acoustic neurofibromatosis

Sound Localisation in Children with a Severe Unilateral Hearing Loss

Progressive sensorineural hearing loss in childhood

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