Hai cercato: elfin

Codice catalogo: (BOSSBS-15270R)

Fornitore: Bioss

Codice articolo fornitore: BS-15270R

Codice articolo locale: BOSSBS-15270R

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15261R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15261R-CY7

Codice articolo locale: BOSSBS-15261R-CY7

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15270R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-15270R-CY7

Codice articolo locale: BOSSBS-15270R-CY7

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15274R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-15274R-HRP

Codice articolo locale: BOSSBS-15274R-HRP

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf57 gene product has been provisionally designated C7orf57 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15279R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-15279R-A350

Codice articolo locale: BOSSBS-15279R-A350

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf64 gene product has been provisionally designated C7orf64 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15269R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-15269R-FITC

Codice articolo locale: BOSSBS-15269R-FITC

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf44 gene product has been provisionally designated C7orf44 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15267R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-15267R-A488

Codice articolo locale: BOSSBS-15267R-A488

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf43 gene product has been provisionally designated C7orf43 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15279R-A750)

Fornitore: Bioss

Codice articolo fornitore: BS-15279R-A750

Codice articolo locale: BOSSBS-15279R-A750

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf64 gene product has been provisionally designated C7orf64 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15279R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15279R-CY3

Codice articolo locale: BOSSBS-15279R-CY3

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf64 gene product has been provisionally designated C7orf64 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15260R-A647)

Fornitore: Bioss

Codice articolo fornitore: BS-15260R-A647

Codice articolo locale: BOSSBS-15260R-A647

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf25 gene product has been provisionally designated C7orf25 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15273R)

Fornitore: Bioss

Codice articolo fornitore: BS-15273R

Codice articolo locale: BOSSBS-15273R

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15264R)

Fornitore: Bioss

Codice articolo fornitore: BS-15264R

Codice articolo locale: BOSSBS-15264R

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf34 gene product has been provisionally designated C7orf34 pending further characterization.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15262R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-15262R-HRP

Codice articolo locale: BOSSBS-15262R-HRP

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf29 gene product has been provisionally designated C7orf29 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15273R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15273R-CY3

Codice articolo locale: BOSSBS-15273R-CY3

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15266R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-15266R-CY3

Codice articolo locale: BOSSBS-15266R-CY3

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterisation.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15273R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-15273R-A488

Codice articolo locale: BOSSBS-15273R-A488

Descrizione: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterised by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterisation.

UOM: 1 * 100 µl

Promo