Aglan, Mona SRefine your research by the most used items
Author / Editor
- Antonarakis, Stylianos (2)
- Makrythanasis, Periklis (2)
- Temtamy, Samia (2)
- Abdalla, Ebtesam (1)
- Al Hait, Sana' (1)
- Al-Allawi, Nasir (1)
- Al-Gazali, Lihadh (1)
- Al-Jasmi, Fatma (1)
- Aliferis, Konstantinos (1)
- Bottani, Armand (1)
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remove all| Title | Authors / Editors | Date | |
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A novel homozygous mutation in FGFR3 causes tall stature, severe lateral tibial deviation, scoliosis, hearing impairment, camptodactyly, and arachnodactyly | Makrythanasis, Periklis; Temtamy, Samia; Aglan, Mona S; Otaify, Ghada A; Antonarakis, Stylianos | 2014 |
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Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families | Makrythanasis, Periklis; Nelis, Mari; Santoni, Federico; Guipponi, Michel; ... Hamamy, Hanan | 2014 |
