Borjeson-Forssman-Lehmann Syndrome: A Novel Pituitary Phenotype Due to Mutation in a Novel Gene

Name: Borjeson-Forssman-Lehmann Syndrome: A Novel Pituitary Phenotype Due to Mutation in a Novel Gene
Creator: M T, Dattani
Keywords: Male, 0301 basic medicine, 0303 health sciences, Fibroblast Growth Factor 8, Gene Expression, Genetic Diseases, X-Linked, Syndrome, Hypopituitarism, Fibroblast Growth Factors, Mice

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 2003Publisher:Walter de Gruyter GmbHJournal:Journal of Pediatric Endocrinology and Metabolism, volume 16 (issn: 0334-018X, eissn: 2191-0251,

Authors: M T, Dattani;

doi: 10.1515/jpem.2003.16.9.1207

pmid: 14714741

Borjeson-Forssman-Lehmann Syndrome: A Novel Pituitary Phenotype Due to Mutation in a Novel Gene

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Keywords

Male, Fibroblast Growth Factor 8, Gene Expression, Genetic Diseases, X-Linked, Syndrome, Hypopituitarism, Fibroblast Growth Factors, Mice, Phenotype, Septo-Optic Dysplasia, Pituitary Gland, Anterior, Growth Hormone, Bone Morphogenetic Proteins, Mutation, Animals, Humans, Abnormalities, Multiple, Signal Transduction, Transcription Factors

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