(Q33675885)

28 July 2017

title

Homozygosity in piebald trait (English)

1 reference

28 July 2017

1 reference

Hultén MA

1

1 reference

28 July 2017

Honeyman MM

series ordinal

2

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28 July 2017

Mayne AJ

series ordinal

3

1 reference

28 July 2017

Tarlow MJ

series ordinal

4

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28 July 2017

language of work or name

English

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publication date

1 September 1987

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

24

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28 July 2017

issue

9

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28 July 2017

page(s)

568-571

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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

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050271

Waardenburg's syndrome associated with total aganglionosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050271

Genetic heterogeneity in the Waardenburg syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050271

Heterogeneity in Waardenburg syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050271

21 June 2018

1 reference

12 December 2020

Pigmentary disorders in association with congenital deafness

1 reference

12 December 2020

Dominance and homozygosity in man

1 reference

12 December 2020

Dominance and homozygosity in man

1 reference

12 December 2020

White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome

1 reference

12 December 2020

Identifiers

PMC publication ID

1050271

1 reference

28 July 2017

1 reference