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Phillipe Schröter

PS

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Publications

3

Citations

141

H-Index

3

Active since

2013

Affiliations

Max Planck Institute for Molecular Genetics(Current)

Charité - Universitätsmedizin Berlin

All India Institute of Medical Sciences

University Medical Center

Berlin-Brandenburger Centrum für Regenerative Therapien

Phillipe Schröter is an author at Max Planck Institute for Molecular Genetics specializing in human genetics, homozygous deletion, and medical genetics.

Publications per year

2013–2014

3

Publications

3

Genotype–phenotype spectrum of PYCR1-related autosomal recessive cutis laxa

Aikaterini Dimopoulou, Björn Fischer‐Zirnsak, Thatjana Gardeitchik et al. · Molecular Genetics and Metabolism · 2013 · 71 citations

, , +8

Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1

Björn Fischer‐Zirnsak, Bert Callewaert, Phillipe Schröter et al. · Molecular Genetics and Metabolism · 2014 · 44 citations · Full text

, , +16

Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1

Claus‐Eric Ott, Björn Fischer‐Zirnsak, Phillipe Schröter et al. · Bone · 2013 · 26 citations

, , +13

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