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Description: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
Catalog Number: BOSSBS-6580R
UOM: 1 * 100 µl
Supplier: Bioss


Description: Defects in GDF5 are the cause of acromesomelic chondrodysplasia Grebe type (AMDG) . Acromesomelic chondrodysplasias are rare hereditary skeletal disorders characterized by short stature, very short limbs, and hand/foot malformations. The severity of limb abnormalities increases from proximal to distal with profoundly affected hands and feet showing brachydactyly and/or rudimentary fingers (knob-like fingers). AMDG is an autosomal recessive form characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of acromesomelic chondrodysplasia Hunter-Thompson type (AMDH). AMDH is an autosomal recessive form of dwarfism. Patients have limb abnormalities, with the middle and distal segments being most affected and the lower limbs more affected than the upper. AMDH is characterized by normal axial skeletons and missing or fused skeletal elements within the hands and feet.Defects in GDF5 are the cause of brachydactyly type C (BDC). BDC is an autosomal dominant disorder characterized by an abnormal shortness of the fingers and toes.
Catalog Number: BOSSBS-6580R-HRP
UOM: 1 * 100 µl
Supplier: Bioss


Description: Potassium sulphate, tablets
Catalog Number: THOMAB40
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER


Description: Potassium sulphate, tablets, PS KJELTABS mineralisation catalyst
Catalog Number: THOMAA23
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: The protein encoded by this gene is a member of the bone morphogenetic protein (BMP) family and the TGF-beta superfamily. This group of proteins is characterized by a polybasic proteolytic processing site which is cleaved to produce a mature protein containing seven conserved cysteine residues. The members of this family are regulators of cell growth and differentiation in both embryonic and adult tissues. Mutations in this gene are associated with acromesomelic dysplasia, Hunter-Thompson type; brachydactyly, type C; and chondrodysplasia, Grebe type. These associations confirm that the gene product plays a role in skeletal development.
Catalog Number: PRSI56-193
UOM: 1 * 400 µl
Supplier: ProSci Inc.

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Description: Sodium sulphate, tablets, KJELTABS NA mineralisation catalyst
Catalog Number: THOMAA40
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: Kjeldahl catalyst reagents in a convenient tablet form with a range of tablets to suit general and specific applications.
Catalog Number: 705-0510
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: KJELTABS SX 1 * 1.000 Tablet
Catalog Number: THOMAA12
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER


Description: KJELTABS KPC 1 * 1.000 Tablet
Catalog Number: THOMAA45
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: SPECIAL KJELTABS AB04 1 * 1.000 Tablet
Catalog Number: THOMAB04
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: SPECIAL KJELTABS AB42 1 * 1.000 Tablet
Catalog Number: THOMAB42
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: SPECIAL KJELTAB AB24 1 * 1.000 Tablet
Catalog Number: THOMAB24
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER


Description: KJELTABS SPECIAL AB61 1 * 1.000 Tablet
Catalog Number: THOMAB61
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER


Description: SPECIAL KJELTAB AB21 1 * 1.000 Tablet
Catalog Number: THOMAB21
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER


Description: KJELTABS IB48 1 * 1.000 Tablet
Catalog Number: THOMAA24
UOM: 1 * 1.000 Tablet
Supplier: THOMPSON & CAPPER

Description: Special Kjeltabs Dairy AB90 6.0 g K2SO4 + 0.025 g CuSO4*5H2O 1 * 500 Tablet
Catalog Number: THOMAB90
UOM: 1 * 500 Tablet
Supplier: THOMPSON & CAPPER

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