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  2. Details for: Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.
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Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. [electronic resource]

By:
  • Delahaye, Andrée
Contributor(s):
  • Khung-Savatovsky, Suonavy
  • Aboura, Azzedine
  • Guimiot, Fabien
  • Drunat, Séverine
  • Alessandri, Jean-Luc
  • Gérard, Marion
  • Bitoun, Pierre
  • Boumendil, Julien
  • Robin, Stéphanie
  • Huel, Chan
  • Guilherme, Romain
  • Serero, Stéphane
  • Gressens, Pierre
  • Elion, Jacques
  • Verloes, Alain
  • Benzacken, Brigitte
  • Delezoide, Anne-Lise
  • Pipiras, Eva
Producer: 20130219Description: 2430-8 p. digitalISSN:
  • 1552-4833
Subject(s):
  • Adult
  • Anterior Eye Segment -- abnormalities
  • Cerebellar Diseases -- genetics
  • Child, Preschool
  • Chromosomes, Human, Pair 6 -- genetics
  • Comparative Genomic Hybridization
  • Dandy-Walker Syndrome -- genetics
  • Eye Abnormalities -- genetics
  • Eye Diseases, Hereditary
  • Female
  • Fetus -- pathology
  • Forkhead Transcription Factors -- genetics
  • Gene Deletion
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Phenotype
  • Pregnancy
Online resources:
  • Available from publisher's website
In: American journal of medical genetics. Part A vol. 158A
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Publication Type: Journal Article

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Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.

APA

Delahaye A., Khung-Savatovsky S., Aboura A., Guimiot F., Drunat S., Alessandri J., Gérard M., Bitoun P., Boumendil J., Robin S., Huel C., Guilherme R., Serero S., Gressens P., Elion J., Verloes A., Benzacken B., Delezoide A. & Pipiras E. (20130219). Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. : American journal of medical genetics. Part A.

Chicago

Delahaye Andrée, Khung-Savatovsky Suonavy, Aboura Azzedine, Guimiot Fabien, Drunat Séverine, Alessandri Jean-Luc, Gérard Marion, Bitoun Pierre, Boumendil Julien, Robin Stéphanie, Huel Chan, Guilherme Romain, Serero Stéphane, Gressens Pierre, Elion Jacques, Verloes Alain, Benzacken Brigitte, Delezoide Anne-Lise and Pipiras Eva. 20130219. Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. : American journal of medical genetics. Part A.

Harvard

Delahaye A., Khung-Savatovsky S., Aboura A., Guimiot F., Drunat S., Alessandri J., Gérard M., Bitoun P., Boumendil J., Robin S., Huel C., Guilherme R., Serero S., Gressens P., Elion J., Verloes A., Benzacken B., Delezoide A. and Pipiras E. (20130219). Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. : American journal of medical genetics. Part A.

MLA

Delahaye Andrée, Khung-Savatovsky Suonavy, Aboura Azzedine, Guimiot Fabien, Drunat Séverine, Alessandri Jean-Luc, Gérard Marion, Bitoun Pierre, Boumendil Julien, Robin Stéphanie, Huel Chan, Guilherme Romain, Serero Stéphane, Gressens Pierre, Elion Jacques, Verloes Alain, Benzacken Brigitte, Delezoide Anne-Lise and Pipiras Eva. Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. : American journal of medical genetics. Part A. 20130219.

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