(Q48455961)

English

A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum.

scientific article published on 8 September 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

Elke Holinski-Feder

2

object named as

Elke Holinski-Feder

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

author name string

Udo Koehler

1

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

Birgit Ertl-Wagner

3

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

Juergen Kunz

4

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

Arpad von Moers

5

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

Hubertus von Voss

6

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

Chayim Schell-Apacik

7

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

publication date

8 September 2009

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

169

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

4

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

463-468

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

https://scigraph.springernature.com/pub.10.1007/s00431-009-1057-2

0 references

Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal Localization of the Four Genes (NFIA, B, C, and X) for the Human Transcription Factor Nuclear Factor I by FISH

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial microdeletion of chromosome 1p in two siblings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization, splice products and mouse chromosomal localization of genes for transcription factor Nuclear Factor One

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/19763616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-009-1057-2

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/19763616

ResearchGate publication ID

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