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Peter Meinecke

University of Hamburg

6

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111

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Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities.

2020 American Journal of Human Genetics
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Biallelic and De Novo Variants in DONSON Reveal a Clinical Spectrum of Cell Cycle‐opathies with Microcephaly, Dwarfism and Skeletal Abnormalities

2019 American Journal of Medical Genetics Part A
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Agnathia, holoprosencephaly, and situs inversus: A third report

1990 American Journal of Medical Genetics
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Smith‐Lemli‐Opitz syndrome

1987 American Journal of Medical Genetics
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Citations (16)