Torthaí cuardaigh - Francesca Vitelli
- 1 - 5 toradh as 5 á dtaispeáint
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TBX1 is required for inner ear morphogenesis de réir Francesca Vitelli, Antonella Viola, Masae Morishima, Tiziano Pramparo, Antonio Baldini, Elizabeth Lindsay
Foilsithe / Cruthaithe 2003Artigo -
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Preserved speech variant is allelic of classic Rett syndrome de réir Cristina De Bona, Michele Zappella, Joussef Hayek, Ilaria Meloni, Francesca Vitelli, Mirella Bruttini, Roberto Cusano, Paola Loffredo, Ilaria Longo, Alessandra Renieri
Foilsithe / Cruthaithe 2000Artigo -
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FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation de réir Monica Piccini, Francesca Vitelli, Mirella Bruttini, Barbara R. Pober, Jón J. Jónsson, Marcello Villanova, Massimo Zollo, Giuseppe Borsani, Andrea Ballabio, Alessandra Renieri
Foilsithe / Cruthaithe 1998Artigo -
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Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice de réir 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
Foilsithe / Cruthaithe 2009Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
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