(Q30495432)

3 October 2017

1 reference

title

PROFOUND CHILDHOOD DEAFNESS. (English)

1 reference

3 October 2017

1 reference

FRASER GR

1

1 reference

PMC publication ID

1012760

3 October 2017

language of work or name

English

0 references

publication date

1 December 1964

1 reference

Journal of Medical Genetics

3 October 2017

1 reference

3 October 2017

1

1 reference

3 October 2017

2

1 reference

3 October 2017

118-151

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

3 October 2017

1 reference

Hereditary 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=1012760

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=1012760

Familial ataxia, deaf-mutism, and muscular wasting

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Multiple congenital anomaly caused by an extra autosome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Sex-linked hereditary 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=1012760

THE METABOLIC ERRORS IN CERTAIN TYPES OF FAMILIAL GOITER

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

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=1012760

VIRUS LESIONS OF THE CRANIAL NERVES WITH SPECIAL REFERENCE TO THE VIII NERVE.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

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=1012760

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=1012760

Gene action in the X-chromosome of the mouse (Mus musculus L.)

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

An English family with Waardenburg's 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=1012760

20 June 2018

The first arch syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Congenital deaf-mutism, prolonged QT interval, syncopal attacks 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=1012760

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=1012760

Optic atrophy and nerve deafness in diabetes mellitus

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Recent work on the biochemistry of the labyrinthine fluids

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

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=1012760

Kernicterus and prematurity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Deafness in cerebral-palsied school-children

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Non-endemic goitrous cretinism

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

A new form of congenital hereditary deafness (Waardenburg's 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=1012760

Perceptive deafness associated with severe neonatal jaundice; a report of 16 cases

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Genetic analysis of the deaf in Hawaii

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

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=1012760

HISTOCHEMICAL STUDIES ON GLYCOGEN IN THE COCHLEA OF THE NORMAL GUINEA PIG.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Multiple anomalies in gongenitally deaf children

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Pathological studies of deafmutes.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Hereditary nerve deafness. A follow-up of four cases in one 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=1012760

Ototoxic medication in premature children

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Deafness and the Treacher Collins 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=1012760

Causes of severe deafness in schoolchildren in Northumberland and Durham

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

The association of deafness with thyroid 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=1012760

Dominant hereditary nerve 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=1012760

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=1012760

Deafness in toxoplasmosis

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Congenital deafness in white cats.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Refsum's syndrome; heredopathia atactica polyneuritiformis; a report of three cases, including a study of the cardiac pathology.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Audiometric and ECG correlations during degenerescence of the pigment layer of the retina; 22 cases; oto-neuro-retinal abiotrophy

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Toxoplasmosis and 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=1012760

Familial association of nerve deafness with nodular goiter and thyroid carcinoma

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Association of congenital deafness with goitre; the nature of the thyroid 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=1012760

Sudden perceptive deafness and viral infection; report of the first one hundred patients

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

A statistical study of 560 cases of the deaf in Peking.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Congenital deafness and goiter

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

The pathology of rubella 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=1012760

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Causes of deafness in young children

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

Hearing impairments in children

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

A newly recognized forme fruste of Hurler's disease (gargoylism)

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1012760

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

[On the problem of intrauterine streptomycin damage]

1 reference

12 December 2020

A deafmute with two congenital syndromes

1 reference

12 December 2020

Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects

1 reference

12 December 2020

Problem of so-called congenital atresia of the ear; histologic report of a new case

1 reference

12 December 2020

Comments on the inheritance of deaf mutism in Northern Ireland

1 reference

12 December 2020

THE TREACHER COLLINS SYNDROME

1 reference

12 December 2020

Hereditary deaf mutism, with particular reference to Northern Ireland

1 reference

12 December 2020

Thalidomide and aplasia-hypoplasia of the otic labyrinth

1 reference

12 December 2020

The Waardenburg syndrome

1 reference

12 December 2020

Pathohistological aural changes in the progeny of a mother with pseudohypoparathyroidism

1 reference

12 December 2020

[A case of Klippel-Feil's syndrome with abducens paralysis; retraction of the eyeball and deaf-mutism]

1 reference

12 December 2020

[A new type of tapeto-retinal degeneration in the course of deaf-mutism]

1 reference

12 December 2020

Hearing and speech disorders in childhood

1 reference

12 December 2020

Deafness Following Maternal Rubella: Retrospective and Prospective Studies

1 reference

12 December 2020

[GOITER DUE TO DEFECTIVE IODINE FIXATION.]

1 reference

12 December 2020

Genetics of the lipidoses

1 reference

12 December 2020

1 reference

12 December 2020

DEQUALINIUM: A POSSIBLE COMPLICATION OF ITS USE IN BALANITIS

1 reference

12 December 2020

[Ogival palate, a so-called sporadic constitutional stigma of deaf-mutism]

1 reference

12 December 2020

WILDERVANCK'S SYNDROME. KLIPPEL-FEIL'S SYNDROME ASSOCIATED WITH DEAFNESS AND RETRACTION OF THE EYEBALL

1 reference

12 December 2020

Hereditary lesions of the labyrinth in the mouse

1 reference

12 December 2020

A note on deaf mutism

1 reference

12 December 2020

MANDIBULO-FACIAL DYSOSTOSIS, ITS CLINICAL ASSOCIATIONS AND HEREDIATRY MECHANISM; REVIEW OF THE RECENT LITERATURE

1 reference

12 December 2020

Waardenbrug's syndrome. A variation of the first arch syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Rubella and Deaf-Mutism in Sweden

1 reference

12 December 2020

[Endocrine status in retinitis pigmentosa with cochleovestibular degeneration]

1 reference

12 December 2020

Retinitis: pigmentosa or rubella

1 reference

12 December 2020

The syndrome of sporadic goitre and congenital deafness

1 reference

12 December 2020

A report of the occurrence of deaf-mutism and goiter in four of six siblings of a North American family

1 reference

12 December 2020

Innate functional defects of the renal tubules, with particular reference to the Fanconi syndrome; cases with retinitis pigmentosa

1 reference

12 December 2020

Identifiers

0 references

1 reference

PMC publication ID

1012760

3 October 2017

PubMed publication ID

14234108

1 reference

PMC publication ID

1012760