Clinical genetic exam 20
Jo
Jo
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Kartei Details
| Karten | 100 |
|---|---|
| Sprache | Deutsch |
| Kategorie | Medizin |
| Stufe | Universität |
| Erstellt / Aktualisiert | 23.02.2020 / 24.02.2020 |
| Lizenzierung | Keine Angabe |
| Weblink |
https://card2brain.ch/box/20200223_clinical_genetic_exam_20
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| Einbinden |
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The following are the most typical faciocranial defects seen in Patau syndrome:
The child with down syndrome:
Who should you refer to a clinical geneticist?
Prader-Willi syndrome is in the MAJORITY of cases caused by:
An individual with 47,XXY karyotype:
Achondroplasia is a genetic disorder with:
The following is TRUE about Smith-Lemli Opitz syndrome
The following statements concerning cystic fibrosis are true EXCEPT:
