16 results on '"Meinecke, P."'
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2. SOX9 mutation in a previously published case of campomelic dysplasia without overt campomelia
3. The cerebro-costo-mandibular syndrome: seven patients and review of the literature
4. Fryns syndrome: two further cases without lateral diaphragmatic defects
5. Desbuquois syndrome
6. Setleis (bitemporal 'forceps marks') syndrome in a German family
7. Campomelic dysplasia without overt campomelia
8. Kabuki make-up (Niikawa-Kuroki) syndrome
9. Microgastria-hypoplastic upper limb association
10. Encephalocele, radial defects, cardiac, gastrointestinal, anal, and renal anomalies
11. A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardation.
12. Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature.
13. A second case of Devriendt syndrome.
14. Familial megalencephaly with dilated Virchow-Robin spaces in magnetic resonance imaging: an autosomal recessive trait?
15. The cerebro-costo-mandibular syndrome: seven patients and review of the literature.
16. The Peters'-Plus syndrome: description of 16 patients and review of the literature.
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