(Q33968872)

30 July 2017

title

Karyotype studies among children with severe visual handicap (English)

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30 July 2017

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Fraser GR

1

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30 July 2017

Friedmann AI

2

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30 July 2017

Delhanty JD

3

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30 July 2017

Edwards JH

4

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30 July 2017

Glen-Bott AM

5

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30 July 2017

Insley J

6

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30 July 2017

Lele KP

7

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30 July 2017

Mittwoch U

8

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30 July 2017

Mutton D

9

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30 July 2017

language of work or name

English

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publication date

1 February 1970

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British Journal of Ophthalmology

30 July 2017

published in

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30 July 2017

volume

54

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30 July 2017

issue

2

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30 July 2017

page(s)

79-89

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CHROMOSOMES IN COLOBOMA AND ANAL ATRESIA

30 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=1207640

THE SYNDROMES OF PSEUDOGLIOMA

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Spontaneous regression of retinoblastoma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Congenital ectodermal dysplasia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Iris dysgenesis with other anomalies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

The 13q-deletion syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Retinoblastoma and deletion D (14) syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Bibliography of Sir Stewart Duke-Elder.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

Choroideremia. Visual defects in a heterozygote

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1207640

A Childhood Syndrome of Bone Dysplasia, Retinal Detachment and Deafness

29 October 2018

1 reference

12 December 2020

HEREDITARY RETINOBLASTOMA

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12 December 2020

CHROMOSOME RESEARCH IN EYE ABNORMALITIES

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12 December 2020

A new syndrome; dyscephalia with bird face and dental anomalies, nanism, hypotrichosis, cutaneous atrophy, microphthalmia, and congenital cataract

1 reference

12 December 2020

CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS

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12 December 2020

XXX 21-trisomy and retinoblastoma

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12 December 2020

Identifiers

DOI

10.1136/BJO.54.2.79

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30 July 2017

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30 July 2017

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