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Literature DB >> 14234108

PROFOUND CHILDHOOD DEAFNESS.

Abstract

Keywords: ADOLESCENCE; CHILD; DEAFNESS; GENETICS, HUMAN; GOITER; HEART DEFECTS, CONGENITAL; RETINITIS PIGMENTOSA; REVIEW; SEX CHROMATIN

Mesh：

Year: 1964 PMID： 14234108 PMCID： PMC1012760 DOI： 10.1136/jmg.1.2.118

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

× No keyword cloud information.

84 in total

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

Authors: G R FRASER; P FROGGATT; T MURPHY
Journal: Ann Hum Genet Date: 1964-11 Impact factor: 1.670

2. Sex-linked hereditary deafness.

Authors: J SATALOFF; P N PASTORE; E BLOOM
Journal: Am J Hum Genet Date: 1955-06 Impact factor: 11.025

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

Authors: L ZIPRKOWSKI; A KRAKOWSKI; A ADAM; H COSTEFF; J SADE
Journal: Arch Dermatol Date: 1962-10

4. Hereditary nerve deafness. A follow-up of four cases in one family.

Authors: F WILLIAMS; L A ROBLEE
Journal: Arch Otolaryngol Date: 1962-01

5. Sex-linked deaf-mutism.

Authors: B W RICHARDS
Journal: Ann Hum Genet Date: 1963-02 Impact factor: 1.670

6. Deafness and the Treacher Collins syndrome.

Authors: C A HOLBOROW
Journal: J Laryngol Otol Date: 1961-11 Impact factor: 1.469

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

Authors: J R SETTELMAYER; M HOGAN
Journal: N Engl J Med Date: 1961-03-09 Impact factor: 91.245

8. Association of congenital deafness with goitre; the nature of the thyroid defect.

Authors: M E MORGANS; W R TROTTER
Journal: Lancet Date: 1958-03-22 Impact factor: 79.321

9. Non-endemic goitrous cretinism.

Authors: A D JACKSON
Journal: Arch Dis Child Date: 1954-12 Impact factor: 3.791

10. Congenital deafness.

Authors: A A VAN EGMOND
Journal: J Laryngol Otol Date: 1954-07 Impact factor: 1.469

18 in total

1. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

Authors: C C Greene; P M McMillan; S E Barker; P Kurnool; M I Lomax; M Burmeister; M M Lesperance
Journal: Am J Hum Genet Date: 2000-12-11 Impact factor: 11.025

2. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors: H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal: Hum Genet Date: 1988-12 Impact factor: 4.132

6. An evaluation of developmental examination as a method of detecting neurological, visual, and auditory handicaps in infancy.

Authors: C J Roberts; T Khosla
Journal: Br J Prev Soc Med Date: 1972-05

PROFOUND CHILDHOOD DEAFNESS.

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

2. Sex-linked hereditary deafness.

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

4. Hereditary nerve deafness. A follow-up of four cases in one family.

5. Sex-linked deaf-mutism.

6. Deafness and the Treacher Collins syndrome.

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

8. Association of congenital deafness with goitre; the nature of the thyroid defect.

9. Non-endemic goitrous cretinism.

10. Congenital deafness.

1. DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

2. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

3. Cervical vertebral fusion (Klippel-Feil) syndrome with consanguineous parents.

4. Hirschsprung's disease and congenital deafness.

5. [Diagnosis of malformations of the ear and temporal bone].

6. An evaluation of developmental examination as a method of detecting neurological, visual, and auditory handicaps in infancy.

Review 7. Inherited diseases of the inner ear in man in the light of studies on the mouse.

8. Familial microtia with meatal atresia in two sibships.

Review 9. Maternal rubella and its effect on the foetus.

10. Family studies of early childhood deafness ascertained through the Clarke School for the Deaf.