Aktuelle Methoden in der Behandlung des unerfüllten ... - ifb
Aktuelle Methoden in der Behandlung des unerfüllten ... - ifb
Aktuelle Methoden in der Behandlung des unerfüllten ... - ifb
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PGD – Suche nach E<strong>in</strong>zelgendefekten<br />
Liste UK: Versuch <strong>der</strong> Regulierung <strong>in</strong> UK<br />
Adrenoleukodystrophy, Agammaglobul<strong>in</strong>aemia, Alpers Syndrome, An<strong>der</strong>son Fabry Disease, Androgen<br />
Insensitivity Syndrome, Autosomal recessive non-syndromic sensor<strong>in</strong>eural deafness, Beckers Muscular<br />
Dystrophy, Beta Hydroxyisobuyryl CoA Hydrolase Deficiency (Methacryic Aciduria), Beta Thalassaemia, Breast<br />
cancer, BRCA 1, Bruton Agammaglobul<strong>in</strong>emia Tyros<strong>in</strong>e K<strong>in</strong>ase (BTK), Cardiac Valvular Dysplasia, Charcot Marie<br />
Tooth Disease, Choroi<strong>der</strong>aemia, Chronic Granulomatous Disease Coff<strong>in</strong>-Lowry Syndrome, Congenital Adrenal<br />
Zystische Fibrose<br />
Muskeldystrophie Duchenne<br />
Fanconi-Anämie<br />
Hyperplasia,· Congenital Fibrosis of the Extraocular Muscles, Crouzon Syndrome, Cystic Fibrosis, Duchenne<br />
Muscular Dystrophy, Early Onset Alzheimers Disease, Ecto<strong>der</strong>mal Dysplasia, Facioscapulohumeral Dystrophy,<br />
Corea Hunt<strong>in</strong>gton<br />
Familial Adenomatous polyposis coli (FAP), Fanconi's Anaemia A, Fanconi's Anaemia C, Fragile X Syndrome,<br />
Gonadal mosaicism, Haemophilia A, Haemophilia B, Hallipeau-Siemens recessive dystrophic epi<strong>der</strong>molysis<br />
bullosa, Homozygous familial Hypercholesterolaemia, Hunters Syndrome, Hunt<strong>in</strong>gton’s Disease (Hunt<strong>in</strong>gton's<br />
Chorea), Hämophilie Hydroxyisobuyryl A CoA Hydrolase Deficiency, Hypogammaglobul<strong>in</strong>aemia, Incont<strong>in</strong>entia Pigmenti, Infantile<br />
Battens Disease, Juvenile Ret<strong>in</strong>oschisis, Lenz syndrome, Lesch Nyan Syndrome, Li-Fraumeni Syndrome,<br />
Lymphoproliferative Syndrome Marfan Syndrome, Marfan Syndrome, Metachromatic Leukodystrophy, Multiple<br />
Endocr<strong>in</strong>e Brustkrebsgen Neoplasia Type 1, Myotonic (BRCA1) Dystrophy, Myotublar myopathy, Myotubular atrophy, Neurofibromatosis<br />
type I, Neurofibromatosis type II, Niemann Pick Disease Type C, Ornith<strong>in</strong>e carbamoyl transferase (OTC)<br />
Deficiency, Ostheopathia Striata with Cranial, Sclerosis (OSCS), Otopalatodigital syndrome type 2, · Partial<br />
Lipodystrophy, Familial, Type 2, Pelizaeus Merzbacher Disease, Pra<strong>der</strong> Willi Syndrome, Severe aplastic anaemia,<br />
Severe Comb<strong>in</strong>ed Immune Deficiency, Sickle Cell Anaemia, Sp<strong>in</strong>al Muscular Atrophy, Tay sachs disease, Treacher<br />
Coll<strong>in</strong>s Syndrome, Von Hippel L<strong>in</strong>dau (VHL) Syndrome, Wiscott-Aldrich Syndrome, X-l<strong>in</strong>ked Hereditary Motor and<br />
Sensory Neuropathies, X-l<strong>in</strong>ked hydrocephalus, X-l<strong>in</strong>ked Immuno-deficiencies, X-l<strong>in</strong>ked Mental Retardation, X-<br />
l<strong>in</strong>ked spastic paraplegia, Chromosomal rearrangements, etc.<br />
Frauenkl<strong>in</strong>ik<br />
Universität-Fortpflanzungszentrum Franken (UFF)<br />
Zertifizierung nach DIN:ISO 9001:2000<br />
63
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