Результати пошуку - Francesca Vitelli
- Показ 1 - 5 результатів із 5
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TBX1 is required for inner ear morphogenesis за авторством Francesca Vitelli, Antonella Viola, Masae Morishima, Tiziano Pramparo, Antonio Baldini, Elizabeth Lindsay
Опубліковано 2003Artigo -
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Preserved speech variant is allelic of classic Rett syndrome за авторством Cristina De Bona, Michele Zappella, Joussef Hayek, Ilaria Meloni, Francesca Vitelli, Mirella Bruttini, Roberto Cusano, Paola Loffredo, Ilaria Longo, Alessandra Renieri
Опубліковано 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 за авторством Monica Piccini, Francesca Vitelli, Mirella Bruttini, Barbara R. Pober, Jón J. Jónsson, Marcello Villanova, Massimo Zollo, Giuseppe Borsani, Andrea Ballabio, Alessandra Renieri
Опубліковано 1998Artigo -
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Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice за авторством 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
Опубліковано 2009Artigo
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Пов'язані теми
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