Votre recherche pour: THOMPSON+

Référence Produit: (BOSSBS-6580R)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (THOMAB40)

Fournisseur: THOMPSON & CAPPER

Description: Potassium sulfate, en comprimés

UOM: 1 * 1.000 Tablet

*Promo

Référence Produit: (BOSSBS-6580R-HRP)

Fournisseur: 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.

UOM: 1 * 100 µl

*Promo

Référence Produit: (THOMAA23)

Fournisseur: THOMPSON & CAPPER

Description: Potassium sulfate, en comprimés, PS KJELTABS catalyseur de minéralisation

UOM: 1 * 1.000 Tablet

Certificats. *Promo

Référence Produit: (PRSI56-193)

Fournisseur: ProSci Inc.

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.

UOM: 1 * 400 µl

*Promo

Référence Produit: (THOMAA40)

Fournisseur: THOMPSON & CAPPER

Description: Sodium sulfate, en comprimés, KJELTABS NA catalyseur de minéralisation

UOM: 1 * 1.000 Tablet

Certificats. *Promo

Fournisseur: THOMPSON & CAPPER

Description: Réactifs de catalyse Kjeldahl sous la forme pratique de comprimés, avec un large éventail de comprimés pour convenir aux applications générales et spécifiques.

Certificats.

Référence Produit: (AESCOK072R)

Fournisseur: Aesculap

Description: SPECULUM NASAL, ST.CLAIR THOMPSON, 64MM 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (AESCOM520R)

Fournisseur: Aesculap

Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.0 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (AESCOK070R)

Fournisseur: Aesculap

Description: SPECULUM NASAL, ST.CLAIR THOMPSON, 38MM 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (AESCOM522R)

Fournisseur: Aesculap

Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.2 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (AESCOM521R)

Fournisseur: Aesculap

Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.1 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (AESCOM523R)

Fournisseur: Aesculap

Description: COUTEAU ANNUL.ST.CLAIR-THOMPSON, FIG.3 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (AESCOK073R)

Fournisseur: Aesculap

Description: SPECULUM NASAL, ST.CLAIR THOMPSON, 76MM 1 * 1 Pce

UOM: 1 * 1 Pce

*Promo

Référence Produit: (THOMAA12)

Fournisseur: THOMPSON & CAPPER

Description: TABLETTE KJELTABS, COMPOSITION: 1,4 G K<SUB>2</SUB>SO<SUB>4</SUB> / 0,1 G SE, TYPE: SX 1 * 1.000 Tablet

UOM: 1 * 1.000 Tablet

*Promo

Référence Produit: (THOMAA45)

Fournisseur: THOMPSON & CAPPER

Description: TABLETTE KJELTABS, COMPOSITION: 4,5 G K<SUB>2</SUB>SO<SUB>4</SUB> / 0,5 G CUSO<SUB>4</SUB>.5 H<SUB>2</SUB>O, TYPE: KPC 1 * 1.000 Tablet

UOM: 1 * 1.000 Tablet

Certificats. *Promo