POU3F4
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Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… … Wikipedia
POU-Gen — Die POU Familie ist eine Gruppe von Transkriptionsfaktoren mit einer hochkonservierten Homöodomäne. Im menschlichen Genom wurden 15 POU Gene gefunden. Das Genom der Modellorganismen Drosophila und Caenorhabditis elegans weist dagegen nur fünf… … Deutsch Wikipedia
Octamer transcription factor — An octamer transcription factor is a transcription factor which binds to the ATTTGCAT sequence.[1] Examples include: Oct 1 POU2F1 Oct 2 POU2F2 Oct 3/4 – POU5F1 Oct 6 – … Wikipedia
POU-Familie — Die POU Familie ist eine Gruppe von Transkriptionsfaktoren mit einer hochkonservierten Homöodomäne. Im menschlichen Genom wurden 15 POU Gene gefunden. Das Genom der Modellorganismen Drosophila und Caenorhabditis elegans weist dagegen nur fünf… … Deutsch Wikipedia
Genetic disorder — For a non technical introduction to the topic, see Introduction to genetics. Genetic disorder Classification and external resources MeSH D030342 A genetic disorder is an illness caused by abnormalities in genes or … Wikipedia
Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E … Wikipedia
Cleft lip and palate — For other uses, see Cleft. Cleft lip and palate Classification and external resources … Wikipedia
Septo-optic dysplasia — Classification and external resources ICD 10 Q04.4 ICD 9 742.2 … Wikipedia
Tietz syndrome — Not to be confused with Tietze syndrome. Tietz syndrome Classification and external resources ICD 10 E70.3 (ILDS E70.358) OMIM 103500 … Wikipedia
Congenital hypothyroidism — Classification and external resources ICD 10 E00, E03.0, E03.1 … Wikipedia