Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome.

Tellier, A L; Amiel, J; Delezoide, A L; Audollent, S; Augé, J; Esnault, D; Encha-Razavi, F; Munnich, A; Lyonnet, S; Vekemans, M; Attié-Bitach, T

Tellier, A L; Amiel, J; Delezoide, A L; Audollent, S; Augé, J; Esnault, D; Encha-Razavi, F; Munnich, A; Lyonnet, S; Vekemans, M; Attié-Bitach, T.

Affiliation

Tellier AL; Département de Génétique et Unité INSERM U-393, Hôpital Necker-Enfants Malades, Paris, France.

Am J Med Genet ; 93(2): 85-8, 2000 Jul 17.

Article in En | MEDLINE | ID: mdl-10869107

Subject(s)

Abnormalities, Multiple/genetics; DNA-Binding Proteins/genetics; Embryo, Mammalian/metabolism; Transcription Factors/genetics; Abnormalities, Multiple/embryology; Abnormalities, Multiple/pathology; Central Nervous System/abnormalities; Central Nervous System/embryology; Coloboma/embryology; Coloboma/pathology; DNA/chemistry; DNA/genetics; DNA Mutational Analysis; Deafness/embryology; Deafness/pathology; Ear/abnormalities; Ear/embryology; Exons; Gene Expression Regulation, Developmental; Humans; In Situ Hybridization; PAX2 Transcription Factor; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Abnormalities, Multiple / DNA-Binding Proteins / Embryo, Mammalian Type of study: Prognostic_studies Limits: Humans Language: En Journal: Am J Med Genet Year: 2000 Document type: Article Affiliation country: France Country of publication: United States

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