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Andreas Tzschach (1972-)

Arzt

Name	Andreas Tzschach
Zeit	1972- (Lebensdaten)
Ort	Altenburg (Geburtsort) Deutschland
Geschlecht	männlich
Beruf	Arzt (charakteristischer Beruf) Humangenetiker
Weitere Angaben	Diss. Fachbereich Humanmedizin, Universität Leipzig. - Habilitation an der Medizinischen Fakultät der Universität Tübingen (Fach Humangenetik)
Datensatztyp	Person
GND-Nummer	122535332
Datensatz-ID	122535332
Beteiligt an alle anzeigen Deep clinical phenotyping of patients with obsessive-compulsive disorder: an approach towards detection of organic causes and first results Aberrant phase separation and nucleolar dysfunction in rare genetic diseases ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways - lessons from breast cancer patients ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways - lessons from breast cancer patients Deep clinical phenotyping of patients with obsessive-compulsive disorder: an approach towards detection of organic causes and first results Adult‐onset neurodegeneration in nucleotide excision repair disorders (NERDND): time to move beyond the skin Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND): Time to Move Beyond the Skin Obsessive–compulsive symptoms in ACTG1-associated Baraitser-Winter cerebrofrontofacial syndrome Marfan syndrome caused by disruption of the FBN1 gene due to a reciprocal chromosome translocation The importance of extended analysis using current molecular genetic methods based on the example of a cohort of 228 patients with hereditary breast and ovarian cancer syndrome Transitioning the molecular tumor board from proof of concept to clinical routine: a german single-center analysis New Cav1.2 channelopathy with high-functioning autism, affective disorder, severe dental enamel defects, a short QT interval, and a novel CACNA1C loss-of-function mutation Einstellungen zu genetischen Untersuchungen bei Medizinstudierenden in den Jahren 2001, 2010 und 2016/17 Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH Molekulargenetische und molekularzytogenetische Untersuchungen bei Patienten mit geistiger Behinderung Molekulargenetische Analyse des Intervall-6 des Y-Chromosoms mittels Sequence-Tagged-Site-PCR bei Patienten mit idiopathischer Oligozoospermie und Azoospermie

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Katalog der Deutschen Nationalbibliothek

Andreas Tzschach (1972-)

Deep clinical phenotyping of patients with obsessive-compulsive disorder: an approach towards detection of organic causes and first results

Aberrant phase separation and nucleolar dysfunction in rare genetic diseases

ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways - lessons from breast cancer patients

ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways - lessons from breast cancer patients

Deep clinical phenotyping of patients with obsessive-compulsive disorder: an approach towards detection of organic causes and first results

Adult‐onset neurodegeneration in nucleotide excision repair disorders (NERDND): time to move beyond the skin

Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND): Time to Move Beyond the Skin

Obsessive–compulsive symptoms in ACTG1-associated Baraitser-Winter cerebrofrontofacial syndrome

Marfan syndrome caused by disruption of the FBN1 gene due to a reciprocal chromosome translocation

The importance of extended analysis using current molecular genetic methods based on the example of a cohort of 228 patients with hereditary breast and ovarian cancer syndrome

Transitioning the molecular tumor board from proof of concept to clinical routine: a german single-center analysis

New Cav1.2 channelopathy with high-functioning autism, affective disorder, severe dental enamel defects, a short QT interval, and a novel CACNA1C loss-of-function mutation

Einstellungen zu genetischen Untersuchungen bei Medizinstudierenden in den Jahren 2001, 2010 und 2016/17

Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH

Molekulargenetische und molekularzytogenetische Untersuchungen bei Patienten mit geistiger Behinderung

Molekulargenetische Analyse des Intervall-6 des Y-Chromosoms mittels Sequence-Tagged-Site-PCR bei Patienten mit idiopathischer Oligozoospermie und Azoospermie