(Q50696880)

17 March 2018

title

Alport's syndrome of hereditary nephritis with deafness. (English)

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17 March 2018

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D A WILLIAMSON

1

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17 March 2018

language of work or name

English

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publication date

1 December 1961

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17 March 2018

number of pages

3

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inferred from page(s)

published in

The Lancet

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17 March 2018

volume

2

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17 March 2018

page(s)

1321-1323

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17 March 2018

issue

7216

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17 March 2018

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

CASE RECORDS of the Massachusetts General Hospital; case 43511

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

Congenital hereditary kidney disease and hearing loss: a case history.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

Hereditary renal dysplasia and blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

A follow-up study of hereditary chronic nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

A clinical study of hereditary interstitial pyelonephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

Congenital hereditary hematuria

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

Hereditary hematuria, nephropathy and deafness; preliminary report.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2861%2990899-6

7 January 2021

10.1016/S0140-6736(61)90899-6

Identifiers

DOI

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17 March 2018

PubMed ID

14007240

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17 March 2018