(Q51791869)

English

Clinical features of incontinentia pigmenti with emphasis on oral and dental abnormalities

scientific article published on 8 August 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

Clinical features of incontinentia pigmenti with emphasis on oral and dental abnormalities (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

author name string

Snezana Minić

1

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

Gerd E K Novotny

2

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

Dusan Trpinac

3

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

Miljana Obradović

4

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

publication date

8 August 2006

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

Clinical Oral Investigations

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

10

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

4

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

343-347

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

Incontinentia pigmenti: XXY male with a family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome: a clinico-genetic study of mentally retarded patients in Kuwait.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Dental anomalies associated with incontinentia pigmenti or Bloch-Sulzberger syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new mutation in exon 7 of NEMO gene: late skewed X-chromosome inactivation in an incontinentia pigmenti female patient with immunodeficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

General and dental characteristics of Bloch-Sulzberger syndrome. Review of literature and presentation of a case report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The half chromatid mutation model and bidirectional mutation in incontinentia pigmenti

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti in four generations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti: a case report.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti. A world statistical analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Incontinentia pigmenti. Study of 3 families]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti: three cases with unusual features

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti: clinicopathologic characteristics and differential diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[From gene to disease; incontinentia pigmenti and the NEMO-gene]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NEMO, NFkappaB signaling and incontinentia pigmenti

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti. A four-generation study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene for incontinentia pigmenti is assigned to Xq28.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti (Bloch-Sulzberger syndrome). A case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incontinentia pigmenti (Bloch-Sulzberger syndrome).

1 reference

https://pubmed.ncbi.nlm.nih.gov/16896835

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00784-006-0066-Z

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16896835

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