Semmola-Meryon-Duchenne syndrome
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- Indbinding:
- Paperback
- Sideantal:
- 64
- Udgivet:
- 20. juli 2018
- Størrelse:
- 150x4x220 mm.
- Vægt:
- 113 g.
- 2-3 uger.
- 16. december 2024
På lager
Forlænget returret til d. 31. januar 2025
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Abonnementspris
- Rabat på køb af fysiske bøger
- 1 valgfrit digitalt ugeblad
- 20 timers lytning og læsning
- Adgang til 70.000+ titler
- Ingen binding
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Ingen binding og kan opsiges når som helst.
- 1 valgfrit digitalt ugeblad
- 20 timers lytning og læsning
- Adgang til 70.000+ titler
- Ingen binding
Abonnementet koster 75 kr./md.
Ingen binding og kan opsiges når som helst.
Beskrivelse af Semmola-Meryon-Duchenne syndrome
There is no satisfactory therapy for many of the disabling genetic disorders such as Semmola-Meryon-Duchenne syndrome. However, it is hoped that advances arising from the accumulating research evidence can contribute to improving treatment of such conditions. Therefore, reviewing the literature for the recent research evidence is recommended to improve the therapeutic services for patients with such disorders. The occurrence of Semmola-Meryon-Duchenne syndrome in Iraq has not been documented. In addition to providing the historical documentation of this syndrome, particularly the early history of its documentation, this book describes the occurrence of Semmola-Meryon-Duchenne syndrome in two Iraqi brothers. This book also reviews the available research evidence which may contribute to improving its treatment.
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