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  2. Details for: Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome.
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Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. [electronic resource]

By:
  • Laffargue, Fanny
Contributor(s):
  • Bourthoumieu, Sylvie
  • Llanas, Brigitte
  • Baudouin, Véronique
  • Lahoche, Annie
  • Morin, Denis
  • Bessenay, Lucie
  • De Parscau, Loïc
  • Cloarec, Sylvie
  • Delrue, Marie-Ange
  • Taupiac, Emmanuelle
  • Dizier, Emilie
  • Laroche, Cécile
  • Bahans, Claire
  • Yardin, Catherine
  • Lacombe, Didier
  • Guigonis, Vincent
Producer: 20150528Description: 259-64 p. digitalISSN:
  • 1468-2044
Subject(s):
  • Adolescent
  • Central Nervous System Diseases -- complications
  • Child
  • Child, Preschool
  • Chromosome Deletion
  • Chromosomes, Human, Pair 17 -- genetics
  • Dental Enamel -- abnormalities
  • Diabetes Mellitus, Type 2 -- complications
  • Female
  • France
  • Hepatocyte Nuclear Factor 1-beta -- genetics
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Kidney Diseases, Cystic -- complications
  • Male
  • Mental Disorders -- genetics
  • Phenotype
  • Prospective Studies
Online resources:
  • Available from publisher's website
In: Archives of disease in childhood vol. 100
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome.

APA

Laffargue F., Bourthoumieu S., Llanas B., Baudouin V., Lahoche A., Morin D., Bessenay L., De Parscau L., Cloarec S., Delrue M., Taupiac E., Dizier E., Laroche C., Bahans C., Yardin C., Lacombe D. & Guigonis V. (20150528). Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. : Archives of disease in childhood.

Chicago

Laffargue Fanny, Bourthoumieu Sylvie, Llanas Brigitte, Baudouin Véronique, Lahoche Annie, Morin Denis, Bessenay Lucie, De Parscau Loïc, Cloarec Sylvie, Delrue Marie-Ange, Taupiac Emmanuelle, Dizier Emilie, Laroche Cécile, Bahans Claire, Yardin Catherine, Lacombe Didier and Guigonis Vincent. 20150528. Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. : Archives of disease in childhood.

Harvard

Laffargue F., Bourthoumieu S., Llanas B., Baudouin V., Lahoche A., Morin D., Bessenay L., De Parscau L., Cloarec S., Delrue M., Taupiac E., Dizier E., Laroche C., Bahans C., Yardin C., Lacombe D. and Guigonis V. (20150528). Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. : Archives of disease in childhood.

MLA

Laffargue Fanny, Bourthoumieu Sylvie, Llanas Brigitte, Baudouin Véronique, Lahoche Annie, Morin Denis, Bessenay Lucie, De Parscau Loïc, Cloarec Sylvie, Delrue Marie-Ange, Taupiac Emmanuelle, Dizier Emilie, Laroche Cécile, Bahans Claire, Yardin Catherine, Lacombe Didier and Guigonis Vincent. Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. : Archives of disease in childhood. 20150528.

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