Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations
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| Veröffentlicht in: | The Pan African medical journal 2012, Vol.11, p.3-3 |
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| container_title | The Pan African medical journal |
| container_volume | 11 |
| creator | Ouldim, Karim Bouguenouch, Laila Samri, Imane El Otmani, Ihsan Hamdaoui, Hasna Bennis, Sanae Lakhdar, Mounia Idrissi Chaouki, Sana Atmani, Samir Hida, Moustapha |
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| fulltext | fulltext |
| identifier | EISSN: 1937-8688 |
| ispartof | The Pan African medical journal, 2012, Vol.11, p.3-3 |
| issn | 1937-8688 |
| language | fre |
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| source | MEDLINE; DOAJ Directory of Open Access Journals; PubMed Central Open Access; African Journals Online (Open Access); EZB-FREE-00999 freely available EZB journals; PubMed Central |
| subjects | 22q11 Deletion Syndrome - diagnosis 22q11 Deletion Syndrome - genetics 22q11 Deletion Syndrome - physiopathology Child Cytogenetics - methods Female Genetic Counseling - methods Humans Infant Williams Syndrome - diagnosis Williams Syndrome - genetics Williams Syndrome - physiopathology |
| title | Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations |
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