x

Zoek een diagnostische test

* (*) verplicht veld

17 Resultaat/Resultaten

Filter op

Specialiteit(en) / Doelstelling(en)

Doel

Landen

Reset
Sorteer op

Titel : Accreditatie =Accreditatie
;

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Huntington Chorea (HTT, Mutation analysis, PGD)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Ichthyosis, X-linked (STS gene)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of PhenylKetonuria (PAH, Mutation analysis, PGD)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Bloom Syndrome (BLM, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Canavan Disease (ASPA, Mutation analysis, Carrier screening, PGD)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Familial Dysautonomia (IKBKAP, Mutation analysis, Carrier screening, PGD)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Fanconi anemia type A (FANCA, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Fanconi Anemia type C (FANCC, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Gaucher disease (GBA, Mutation analysis, Carrier detection)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Glycogen Storage disease Ia (G6Pase, Mutation analysis, Carrier screening, PGD)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Limb-Girdle Muscular Dystrophy (DYSF, Mutation analysis, Carrier detection)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Maple Syrup Urine Disease- MSUD (BCKDHB, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Metachromatic leukodystrophy (ARSA, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Mucolipidosis Type IV (MCOLN1, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Nemaline myopathy (NEB, Mutation analysis, Carrier screening, PGD)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Niemann Pick -Type A (SMPD1, Mutation analysis, Carrier screening)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica

ISRA╦L

ISRAEL
RAMAT GAN

Molecular diagnosis of Deafness (mitochondrial) (MTRNR1)
Sheba Medical Center
Doelstelling(en) : Postnatale diagnose
Specialiteit(en) : Moleculaire genetica