Каталог анализов

Вы отложили "Alport syndrome and disorders of glomerular basement membrane (GBM)" в свою корзину. Просмотр корзины

Hearing loss, nonsyndromic, autosomal recessive and X-linked
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Hearing loss, nonsyndromic, autosomal dominant and X-linked
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Syndromic hearing loss
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Familial and idiopathic epilepsy
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Epilepsy and developmental delay (incl. epileptic encephalopathies)
€1,400.00 Laboratory:
CeGaT (DE)В корзину
GPI anchor deficiency with or without hyperphosphatasia
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Migraine
€950.00 Laboratory:
CeGaT (DE)В корзину
Hyperekplexia
€950.00 Laboratory:
CeGaT (DE)В корзину
Metabolic/Mitochondrial epilepsy
€1,400.00 Laboratory:
CeGaT (DE)В корзину
WES Classic (Blut-Probe) Exome Sequencing
€690.00 Laboratory:
CeGaT (DE)В корзину
WES Premium (Tumor Probe) Sequencing
€1,360.00 Laboratory:
CeGaT (DE)В корзину
Whole Exome Analysis
€1,700.00 Laboratory:
CeGaT (DE)В корзину
Trio Exome Analysis
€2,400.00 Laboratory:
CeGaT (DE)В корзину
Clinical Trio Exome Analysis
€2,200.00 Laboratory:
CeGaT (DE)В корзину
Duo Exome Analysis
€2,200.00 Laboratory:
CeGaT (DE)В корзину
Usher syndrome
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Retinitis pigmentosa, autosomal dominant and X-linked
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Retinitis pigmentosa, autosomal recessive and X-linked
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Bardet-Biedl syndrome
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Congenital stationary night blindness
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Joubert syndrome
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Leber congenital amaurosis
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Zellweger syndrome spectrum (Refsum/ Zellweger/neonatal adrenoleukodystrophy)
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Senior Loken syndrome
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Stargardt disease and macular dystrophies
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Cone rod dystrophies
€1,400.00 Laboratory:
CeGaT (DE)В корзину
Flecked retina disorders
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Vitreoretinopathies (Wagner syndrome/ Norrie/ Coats)
€1,250.00 Laboratory:
CeGaT (DE)В корзину
Stickler syndrome
€950.00 Laboratory:
CeGaT (DE)В корзину
Optic atrophy (incl. LHON (Leber Hereditary Optic Neuropathy))
€1,250.00 Laboratory:
CeGaT (DE)В корзину

Каталог анализов

Hearing loss, nonsyndromic, autosomal recessive and X-linked

Hearing loss, nonsyndromic, autosomal dominant and X-linked

Syndromic hearing loss

Familial and idiopathic epilepsy

Epilepsy and developmental delay (incl. epileptic encephalopathies)

GPI anchor deficiency with or without hyperphosphatasia

Migraine

Hyperekplexia

Metabolic/Mitochondrial epilepsy

WES Classic (Blut-Probe) Exome Sequencing

WES Premium (Tumor Probe) Sequencing

Whole Exome Analysis

Trio Exome Analysis

Clinical Trio Exome Analysis

Duo Exome Analysis

Usher syndrome

Retinitis pigmentosa, autosomal dominant and X-linked

Retinitis pigmentosa, autosomal recessive and X-linked

Bardet-Biedl syndrome

Congenital stationary night blindness

Joubert syndrome

Leber congenital amaurosis

Zellweger syndrome spectrum (Refsum/ Zellweger/neonatal adrenoleukodystrophy)

Senior Loken syndrome

Stargardt disease and macular dystrophies

Cone rod dystrophies

Flecked retina disorders

Vitreoretinopathies (Wagner syndrome/ Norrie/ Coats)

Stickler syndrome

Optic atrophy (incl. LHON (Leber Hereditary Optic Neuropathy))