(Q30495431)

31 October 2017

1 reference

title

Inherited diseases of the inner ear in man in the light of studies on the mouse (English)

1 reference

31 October 2017

1 reference

23 March 2023

author name string

M. S. Deol

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4972661

23 March 2023

language of work or name

English

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publication date

1 June 1968

1 reference

PMC publication ID

1468516

full work available at URL

31 October 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4972661/pdf/?tool=EBI

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4972661

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/4972661/?tool=EBI

23 March 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4972661

https://europepmc.org/articles/PMC1468516

23 March 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4972661

https://europepmc.org/articles/PMC1468516?pdf=render

23 March 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4972661

https://syndication.highwire.org/content/doi/10.1136/jmg.5.2.137

23 March 2023

1 reference

Journal of Medical Genetics

23 March 2023

published in

1 reference

31 October 2017

5

1 reference

31 October 2017

2

1 reference

31 October 2017

137-158

1 reference

Abnormal Segregation in Hereditary Renal Disease with Deafness

31 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

The Inheritance and Expression of Fused, a New Mutation in the House Mouse

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

The Origin of Jerker, a New Gene Mutation of the House Mouse, and Linkage Studies Made with It

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

A New Gene Affecting Behavior and Skeleton in the House Mouse

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Hereditary sensory radicular neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

The placodal relations of the neural crest in the domestic cat

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

PROFOUND CHILDHOOD DEAFNESS.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

HEARING DEGENERATION IN SHAKER-1 MOUSE. CORRELATION OF PHYSIOLOGICAL OBSERVATIONS WITH BEHAVIORAL RESPONSES AND WITH COCHLEAR ANATOMY

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

CONGENITAL DEAFNESS ASSOCIATED WITH ELECTROCARDIOGRAPHIC ABNORMALITIES, FAINTING ATTACKS AND SUDDEN DEATH. A RECESSIVE SYNDROME

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

RECESSIVE TOTAL ALBINISM AND CONGENITAL DEAF-MUTISM.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

A syndrome of deaf-mutism associated with albinism showing dominant autosomal inheritance

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Congenital deafness associated with onychodystrophy.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

A genetic study of hereditary renal dysfunction with associated nerve deafness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Deafness as part of an hereditary syndrome.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Sex-linked deafness of a possibly new type.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Congenital deafness due to a sex-linked recessive gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Hearing and vision in neurological mutant mice: A method for their evaluation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

A neuroectodermal syndrome of dominant inheritance

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

OBSERVATIONS ON THE HISTOLOGICAL FEATURES, DEVELOPMENT AND PATHOGENESIS OF THE INNER EAR DEGENERATION OF THE DEAF WHITE CAT.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

CONGENITAL DEAFNESS AND GOITER. STUDIES OF A PATIENT WITH A COCHLEAR DEFECT AND INADEQUATE FORMATION OF IODOTHYRONINES.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

HEREDITARY PHOTOMYOCLONUS ASSOCIATED WITH DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRAL DYSFUNCTION.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

WAARDENBURG'S SYNDROME WITH DEAFNESS AS THE PRESENTING SYMPTOM. REPORT OF TWO CASES

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

PERCEPTIVE DIAFNESS ASSOCIATED WITH SPLIT-HAND AND -FOOT, A NEW SYNDROME?

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Alport's syndrome of hereditary nephritis with deafness.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Deafness with sporadic goiter. Pendred's syndrome.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Hereditary nephropathy, deafness and renal foam cells.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Waardenburg's syndrome--report of a case in a non-Dutch family.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

The pathology of congenital deafness.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Familial deafness and goitre in persons with a low serum level of protein-bound iodine: preliminary report.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Ectodermal dysplasia; report of kindred with ocular abnormalities and hearing defect.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Vestibular function in deafness and severe hardness of hearing.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468516

26 November 2018

Sex-linked deaf-mutism

1 reference

12 December 2020

Partial albinism and deaf-mutism due to a recessive sex-linked gene

1 reference

12 December 2020

Neurological Defect: Manganese in Phenocopy and Prevention of a Genetic Abnormality of Inner Ear

1 reference

12 December 2020

The melanocytes of mammals

1 reference

12 December 2020

Comments on the inheritance of deaf mutism in Northern Ireland

1 reference

12 December 2020

Hereditary deaf mutism, with particular reference to Northern Ireland

1 reference

12 December 2020

Inner ear pathology due to measles

1 reference

12 December 2020

The origin of the acoustic ganglion in the sheep

1 reference

12 December 2020

Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse

1 reference

12 December 2020

HEREDITARY NEPHRITIS. REPORT OF A KINDRED

1 reference

12 December 2020

1 reference

12 December 2020

The development of piebald spotting in mice

1 reference

12 December 2020

The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome)

1 reference

12 December 2020

COCHLEAR POTENTIALS AND 8 NERVE ACTION POTENTIALS IN NORMAL AND GENETICALLY DEAF MICE

1 reference

12 December 2020

Labyrinthine disease in identical twins.

1 reference

12 December 2020

[Morphological and microscopic anatomical studies on the inner ear of a species of spontaneously mutant house mice (turning mice)]

1 reference

12 December 2020

Morphology and behavior of Waltzertype mice

1 reference

12 December 2020

A note on deaf mutism

1 reference

12 December 2020

Hereditary absence of otoliths in the house mouse

1 reference

12 December 2020

A new gene affecting the morphogenesis of the vestibular part of the inner ear in the mouse

1 reference

12 December 2020

Congenital heart disease, deaf-mutism and associated somatic malformations occurring in several members of one family

1 reference

12 December 2020

A New Hereditary Syndrome – Sex-linked Deaf-mutism Associated with Total Albinism

1 reference

12 December 2020

Malformations, anomalies, and vestigial structures of the inner ear

1 reference

12 December 2020

Manganese deficiency in rats: congenital nature of ataxia

1 reference

12 December 2020

Studies on megacolon in piebald mice

1 reference

12 December 2020

The syndrome of sporadic goitre and congenital deafness

1 reference

12 December 2020

Association of Megacolon with Two Recessive Spotting Genes in the Mouse

1 reference

12 December 2020

Inner ear pathology following maternal rubella

1 reference

12 December 2020

The syndrome of Waardenburg

4

1 reference

Observations on the Histological Features, Development and Pathogenesis of the Inner Ear Degeneration of the Deaf White Cat

23 March 2023

13

1 reference

The probable mode of gene action in the circling mutants of the mouse

23 March 2023

26

1 reference

Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness

23 March 2023

42

1 reference

Hereditary lesions of the labyrinth in the mouse

23 March 2023

50

1 reference

Anomalous Development of Ossification in the Inner Ear of Offspring of Manganese-Deficient Rats

23 March 2023

67

1 reference

Further studies on the auditory vesicle and cartilaginous capsule of Amblystoma punctatum

23 March 2023

72

1 reference

The Defective Organ of Corti in Shaker-1 Mice

23 March 2023

73

1 reference

Retinal Degeneration and Nerve Deafness

23 March 2023

79

1 reference

FAMILIAL MYOCLONUS EPILEPSY ASSOCIATED WITH DEAF-MUTISM IN A FAMILY SHOWING OTHER PSYCHOBIOLOGICAL ABNORMALITIES

23 March 2023

80

1 reference

Twirler: a mutant affecting the inner ear of the house mouse

23 March 2023

91

1 reference

23 March 2023

DEAF-MUTISM AND GOITRE

105

1 reference

A gene causing ocular retardation in the mouse

23 March 2023

120

1 reference

THE DETERMINATION OF THE AUDITORY PLACODE IN THE CHICK

23 March 2023

123

1 reference

23 March 2023

Identifiers

0 references

1 reference

PMC publication ID

1468516

31 October 2017

1 reference

PMC publication ID

1468516