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Medientyp
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- Meinecke, Peter
- Rauch, Anita
- Alawi, Malik 1
- Azzarello-Burri, Silvia 1
- Barker, Emma L 1
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Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities
- Schneeberger, Pauline E
- von Elsner, Leonie
- Barker, Emma L
- Meinecke, Peter
- Marquardt, Iris
- Alawi, Malik
- Steindl, Katharina
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Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap.
- Harmsen, May-Britt
- Azzarello-Burri, Silvia
- González, García
- Mar, M
- Gillessen-Kaesbach, Gabriele
- Meinecke, Peter
- Müller, Dietmar