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Detlev Schindler

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X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.

2016 Clinical Dysmorphology
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Spectral karyotyping of Werner syndrome fibroblast cultures.

2000 Cytogenetic and Genome Research
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Isolation and structural characterization of sialic-acid-containing glycopeptides of the O-glycosidic type from the urine of two patients with an hereditary deficiency in alpha-N-acetylgalactosaminidase activity.

1989 Biological chemistry Hoppe-Seyler
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