References in periodicals archive ?
Aarskog-Scott syndrome is an X-linked condition caused by mutations of the FGD1 gene.
Research into FGD1 founder mutations might be usefully conducted in future studies.
Unusually severe expression of craniofacial features in Aarskog-Scott syndrome due to a novel truncating mutation of the FGD1 gene.
MLK3 regulates bone development downstream of the faciogenital dysplasia protein FGD1 in mice.
The belief that they had been able to conceive by taking the medicines from TH was echoed by many participants of both FGD1 and FGD2, including educated, semi-educated and uneducated participants.
The same belief of getting the tidal water for easing the process of the delivery was echoed among the participants of FGD1.
In this connection, the participants of FGD1 stated that their new born child will be taken away by 'Chora Chunni' (mythical malicious spirits) if they do not stay in-door for forty days.
Medical browser ?
Full browser ?