(Q34737921)

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Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder

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scholarly article

1 reference

Europe PubMed Central

4 August 2017

Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder (English)

1 reference

Europe PubMed Central

4 August 2017

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1 reference

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author name string

Chudley AE

1

1 reference

Europe PubMed Central

4 August 2017

McCullough C

2

1 reference

Europe PubMed Central

4 August 2017

McCullough DW

3

1 reference

Europe PubMed Central

4 August 2017

publication date

1 January 1997

1 reference

Europe PubMed Central

4 August 2017

American Journal of Medical Genetics Part A

1 reference

Europe PubMed Central

4 August 2017

68

1 reference

Europe PubMed Central

4 August 2017

3

1 reference

Europe PubMed Central

4 August 2017

350-356

1 reference

Europe PubMed Central

4 August 2017

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

1 reference

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21 January 2018

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

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21 January 2018

Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families

1 reference

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21 January 2018

Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175.

1 reference

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21 January 2018

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

1 reference

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21 January 2018

Autosomal recessive hydrocephalus with third ventricle obstruction

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21 January 2018

Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families

1 reference

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21 January 2018

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

1 reference

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21 January 2018

Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q.

1 reference

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21 January 2018

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

1 reference

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21 January 2018

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene

1 reference

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21 January 2018

Importance of the size of the stoma in choledocho-duodenostomy

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21 January 2018

The gene for an inherited form of deafness maps to chromosome 5q31

1 reference

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21 January 2018

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

1 reference

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21 January 2018

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

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21 January 2018

Current prognosis in overt neonatal hydrocephalus

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21 January 2018

Genetic epidemiology of hearing impairment

1 reference

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21 January 2018

X-linked deafness, stapes gushers and a distinctive defect of the inner ear.

1 reference

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21 January 2018

Genetic deafness

1 reference

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21 January 2018

The genetics of deafness

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21 January 2018

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

1 reference

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21 January 2018

Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15.

1 reference

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21 January 2018

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

1 reference

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21 January 2018

Unilateral hydrocephalus secondary to congenital atresia of the foramen of Monro. Case report.

1 reference

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21 January 2018

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

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A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22-23

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Perinatal unilateral hydrocephalus. Atresia of the foramen of Monro

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Hydrocephalus as a sequela of experimental myxovirus infections

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

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21 January 2018

Identifiers

10.1002/(SICI)1096-8628(19970131)68:3<350::AID-AJMG19>3.0.CO;2-S

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

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