(Q75251208)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

title

Coffin-Lowry syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

author name string

Sanjeev R Ahuja

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

Shubhangi Upadhye

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

Hemant V Kulkarni

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

Madhuri V Kulkarni

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

publication date

1 December 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

Indian Journal of Pediatrics

17 November 2019

published in

1 reference

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17 November 2019

volume

70

1 reference

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17 November 2019

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

page(s)

1001-1002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14719793%20AND%20SRC:MED&resulttype=core&format=json

The Coffin-Lowry syndrome. Experience from four centres.

17 November 2019

cites work

1 reference

12 December 2020

Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome

1 reference

12 December 2020

A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus.

1 reference

12 December 2020

Drop episodes in Coffin-Lowry syndrome: an unusual type of startle response

1 reference

12 December 2020

Cardiac involvement in Coffin-Lowry syndrome.

1 reference

12 December 2020

The Coffin-Lowry syndrome: a simply inherited trait comprising mental retardation, faciodigital anomalies and skeletal involvement

1 reference

12 December 2020