Characterization of a de Novo 43-bp Deletion of the Gsα Gene (GNAS1) in Albright Hereditary Osteodystrophy

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Veröffentlicht in:	Genomics (San Diego, Calif.) Calif.), 1994-05, Vol.21 (2), p.455-457
Hauptverfasser:	Luttikhuis, Monique E.M.Oude, Wilson, Louise C., Leonard, James V., Trembath, Richard C.
Format:	Artikel
Sprache:	eng
Schlagworte:	Base Sequence Biological and medical sciences Chromosomes, Human, Pair 20 Diseases of the osteoarticular system DNA Primers Exons Female Gene Rearrangement GTP-Binding Proteins - genetics Humans Male Malformations and congenital and or hereditary diseases involving bones. Joint deformations Medical sciences Molecular Sequence Data Pedigree Point Mutation Polymerase Chain Reaction - methods Pseudohypoparathyroidism - genetics Sequence Deletion
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