Результаты поиска - Francesca Vitelli
- Отображение 1 - 5 результаты of 5
-
1
-
2
TBX1 is required for inner ear morphogenesis по Francesca Vitelli, Antonella Viola, Masae Morishima, Tiziano Pramparo, Antonio Baldini, Elizabeth Lindsay
Опубликовано 2003Artigo -
3
-
4
FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation по Monica Piccini, Francesca Vitelli, Mirella Bruttini, Barbara R. Pober, Jón J. Jónsson, Marcello Villanova, Massimo Zollo, Giuseppe Borsani, Andrea Ballabio, Alessandra Renieri
Опубликовано 1998Artigo -
5
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice по Victoria Randall, Karen McCue, Catherine Roberts, Vanessa Kyriakopoulou, Sarah Beddow, Angela N. Barrett, Francesca Vitelli, Katrina Prescott, Charles Shaw‐Smith, Koenraad Devriendt, Erika A. Bosman, Georg Steffes, Karen P. Steel, Subreena Simrick, M. Albert Basson, Elizabeth Illingworth, Peter Scambler
Опубликовано 2009Artigo
Инструменты поиска:
Связанные темы
Biology
Gene
Genetics
Phenotype
Gene expression
Haploinsufficiency
Promoter
TBX1
Allele
Anatomy
Cell biology
Morphogenesis
Neural crest
Neuroscience
Alport syndrome
Ataxia
Atresia
CHARGE syndrome
Choanal atresia
Cochlea
Coloboma
DiGeorge syndrome
Ectoderm
Embryogenesis
Epithelium
Fetus
Glomerulonephritis
Heterozygote advantage
Holoprosencephaly
Inner ear