Review on PAX3 (paired box gene 3 (Waardenburg syndrome 1)), with data on DNA, on the protein encoded, and where the gene is implicated
Pax-3 is a transcription factors important in normal embryonic development, as highlighted by its mu...
International audienceWaardenburg syndrome (WS) is characterized by the association of pigmentation ...
Contains fulltext : 21639___.PDF (publisher's version ) (Open Access
Purpose: Screening of mutations in the paired box 3 (PAX3) gene in three generations of a Turkish fa...
Review on PAX5 (paired box gene 5), with data on DNA, on the protein encoded, and where the gene is ...
On some occasions, mutations of a gene cause different syndromes that may have similar phenotypes. F...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg's syndrome (WS) is an autosomal dominant combination of deafness and pigmentary disturba...
Review on PAX6 (paired box 6), with data on DNA, on the protein encoded, and where the gene is impli...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
We describe two different novel mutations in the PAX3 gene, detected in two families with cases of W...
We describe two different novel mutations in the PAX3 gene, detected in two families with cases of W...
Pax-3 is a transcription factors important in normal embryonic development, as highlighted by its mu...
International audienceWaardenburg syndrome (WS) is characterized by the association of pigmentation ...
Contains fulltext : 21639___.PDF (publisher's version ) (Open Access
Purpose: Screening of mutations in the paired box 3 (PAX3) gene in three generations of a Turkish fa...
Review on PAX5 (paired box gene 5), with data on DNA, on the protein encoded, and where the gene is ...
On some occasions, mutations of a gene cause different syndromes that may have similar phenotypes. F...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg's syndrome (WS) is an autosomal dominant combination of deafness and pigmentary disturba...
Review on PAX6 (paired box 6), with data on DNA, on the protein encoded, and where the gene is impli...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
Waardenburg syndrome (WS) is a group of autosomal-dominant hereditary conditions with a global incid...
We describe two different novel mutations in the PAX3 gene, detected in two families with cases of W...
We describe two different novel mutations in the PAX3 gene, detected in two families with cases of W...
Pax-3 is a transcription factors important in normal embryonic development, as highlighted by its mu...
International audienceWaardenburg syndrome (WS) is characterized by the association of pigmentation ...
Contains fulltext : 21639___.PDF (publisher's version ) (Open Access
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