(Q24316386)

lacrimal gland development

GOA release 2020-03-11

1 reference

familial congenital nasolacrimal duct obstruction

GOA release 2020-03-11

1 reference

M Tekin

10

0 references

author name string

J Foster

1

0 references

S Kapoor

2

0 references

O Diaz-Horta

3

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A Singh

4

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C Abad

5

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A Rastogi

6

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R Moharana

7

0 references

O Tekeli

8

0 references

K Walz

Prevalence and clinical characteristics of congenital dacryocystocele

9

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language of work or name

English

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publication date

December 2014

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published in

Clinical Genetics

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volume

86

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issue

6

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page(s)

589-91

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cites work

1 reference

Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss

21 January 2018

1 reference

Autozygosity mapping with exome sequence data

21 January 2018

1 reference

Congenital nasolacrimal duct cyst/dacryocystocele: An argument for a genetic basis

21 January 2018

1 reference

Congenital dacryocystocele: is there a familial predisposition?

21 January 2018

1 reference

Surgical treatment of familial dacryocystocele and lacrimal puncta agenesis.

21 January 2018

1 reference

Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13.

21 January 2018

1 reference

The zebrafish down syndrome cell adhesion molecule is involved in cell movement during embryogenesis.

21 January 2018

1 reference