نتایج جستجو برای: ectrodactyly
تعداد نتایج: 300 فیلتر نتایج به سال:
Journal:
:Veteriner Hekimler Derneği Dergisi
2021
Journal:
:Indian journal of dermatology, venereology and leprology
2012
Adone Baroni
Vincenzo Piccolo
Rosa Di Maio
Teresa Russo
2016
Daniele Conte
Giulia Garaffo
Nadia Lo Iacono
Stefano Mantero
Stefano Piccolo
Michelangelo Cordenonsi
David Perez-Morga
Valeria Orecchia
Valeria Poli
Giorgio R. Merlo
The congenital malformation split hand/foot (SHFM) is characterized by missing central fingers and dysmorphology or fusion of the remaining ones. Type-1 SHFM is linked to deletions/rearrangements of the DLX5-DLX6 locus and point mutations in the DLX5 gene. The ectrodactyly phenotype is reproduced in mice by the double knockout (DKO) of Dlx5 and Dlx6. During limb development, the apical ectoderm...
Journal:
:Journal of Medical Genetics
2011
Journal:
:Pediatrics & Therapeutics
2016
Journal:
:International Journal of Oral and Maxillofacial Surgery
2017
Journal:
:American Journal of Perinatology Reports
2016
Journal:
:American Journal of Medical Genetics Part A
2009
Journal:
:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
2010
Journal:
:Arquivos Brasileiros de Oftalmologia
2018
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید