Sprechstunden/ Spezialsprechstunden am MGZ
Kürzlich hinzugefügt
Umfassendes Spektrum in der Pränatalmedizin
Vortrag: Genetische Diagnostik bei Fruchtwasseranomalien
Vortrag: Pränatale genetische Diagnostik – stepwise approach
Cancer Surveillance Guideline for individuals with PTEN hamartoma
Guidelines for the Li-Fraumeni and Heritable TP53-related Cancer Syndr
Cancer Risks in Lynch Syndrome, Lynch-like Syndrome, and Familial
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk
Analysis of 3297 individuals suggests that the pathogenic germline
Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II:
Genotype‐phenotype correlation in a novel ABHD12 mutation underlying
Critical assessment of secondary findings in genes linked to primary
Delineating MT-ATP6-associated disease: From isolated neuropathy to
ATP1A3-related epilepsy: Report of seven cases and literature-based an
Cooccurrence of Two Different Genetic Diseases: A Case of Valproic
Prevalence of CNV-neutral structural genomic
MGZ-Symposium 2020: Elektrolytstörungen
MGZ-Symposium 2020: Fettstoffwechselstörungen
MGZ-Symposium 2020: Mikrohämaturie
MGZ-Symposium 2020: Erhöhte Leberwerte
MGZ-Symposium 2020: Programm
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Publikationen derzeitiger MGZ-Mitarbeiter / unter Mitwirkung des MGZ
Vortrag: Genetische Diagnostik bei Fruchtwasseranomalien...
Vortrag: Pränatale genetische Diagnostik – stepwise approach
Cancer Risks in Lynch Syndrome, Lynch-like Syndrome, and Familial...
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk...
Analysis of 3297 individuals suggests that the pathogenic germline...
Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II:...
Genotype‐phenotype correlation in a novel ABHD12 mutation underlying...
Critical assessment of secondary findings in genes linked to primary...
Delineating MT-ATP6-associated disease: From isolated neuropathy to...
ATP1A3-related epilepsy: Report of seven cases and literature-based an...
Cooccurrence of Two Different Genetic Diseases: A Case of Valproic...
Prevalence of CNV-neutral structural genomic...
MGZ-Symposium 2020: Programm
Impact on Clinical Decision Making of Next-Generation Sequencing in...
Targeted deep-intronic sequencing in a cohort of unexplained cases of...
Results of multigene panel testing in familial cancer cases without...
Empfehlungen zur Früherkennung, Risikoreduktion, Überwachung und...
A Novel Gain-of-Function Nav1.9 Mutation in a Child With Episodic Pain...
Genetic Screening and Personalized Prevention in Colorectal Cancer...
Cancer risks by gene, age & gender in 6350 carriers of pathogenic...
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Onkologie
Cancer Surveillance Guideline for individuals with PTEN hamartoma...
Guidelines for the Li-Fraumeni and Heritable TP53-related Cancer Syndr...
Cancer Risks in Lynch Syndrome, Lynch-like Syndrome, and Familial...
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk...
Analysis of 3297 individuals suggests that the pathogenic germline...
Prevalence of CNV-neutral structural genomic...
Targeted deep-intronic sequencing in a cohort of unexplained cases of...
Results of multigene panel testing in familial cancer cases without...
Empfehlungen zur Früherkennung, Risikoreduktion, Überwachung und...
Genetic Screening and Personalized Prevention in Colorectal Cancer...
Cancer risks by gene, age & gender in 6350 carriers of pathogenic...
The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome...
Lack of association between screening interval and cancer stage...
MGZ-Symposium 2019: Polyposis - Syndrome
MGZ-Symposium 2019: Psycho-Onkologie
MGZ-Symposium 2019: Das MDK-Gutachten, wie entscheidet der MDK?
MGZ-Symposium 2019: Nationales Sequenzierzentrum - was dürfen wir...
MGZ-Symposium 2019
MGZ-Symposium 2019: Other BC-genes
MGZ-Symposium 2019: Stellenwert prophylaktischer Chirurgie
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Neurologie
Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II:...
Genotype‐phenotype correlation in a novel ABHD12 mutation underlying...
Delineating MT-ATP6-associated disease: From isolated neuropathy to...
ATP1A3-related epilepsy: Report of seven cases and literature-based an...
MGZ-Symposium 2020: Programm
Impact on Clinical Decision Making of Next-Generation Sequencing in...
A Novel Gain-of-Function Nav1.9 Mutation in a Child With Episodic Pain...
VLDLR-associated Pontocerebellar Hypoplasia with Nonprogressive...
Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of t...
Characteristic clinical and ultrastructural findings in nesprinopathie...
Congenital myasthenic syndrome caused by novel COL13A1 mutations...
Kongenitale myasthene Syndrome im Erwachsenenalter...
A nomenclature and classification for the congenital myasthenic...
Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia
LAMA2 gene mutation update: Toward a more comprehensive picture of the...
Hereditary neuralgic amyotrophy in childhood caused by duplication...
Kongenitale myasthene Syndrome im Erwachsenenalter...
The Curse of Apneic Spells...
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MGZ-Symposium 2019
MGZ-Symposium 2019: Polyposis - Syndrome
MGZ-Symposium 2019: Psycho-Onkologie
MGZ-Symposium 2019: Das MDK-Gutachten, wie entscheidet der MDK?
MGZ-Symposium 2019: Nationales Sequenzierzentrum - was dürfen wir...
MGZ-Symposium 2019
MGZ-Symposium 2019: Other BC-genes
MGZ-Symposium 2019: Stellenwert prophylaktischer Chirurgie
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