Find link

language:

Find link is a tool written by Edward Betts.

Longer titles found: Pierre Robin sequence-faciodigital anomaly syndrome (view)

searching for Pierre Robin sequence 6 found (22 total)

Hearing loss with craniofacial syndromes (1,485 words) [view diff] exact match in snippet view article find links to article

malformed or missing ossicles (Pron et al., 1993). Persons with Pierre Robin sequence (PRS) are at greater risk for hearing impairment than persons with

RBM10 (5,530 words) [view diff] no match in snippet view article find links to article

RNA-binding motif 10 is a protein that is encoded by the RBM10 gene. This gene maps on the X chromosome at Xp11.23 in humans. RBM10 is a regulator of alternative

Facies (medical) (378 words) [view diff] exact match in snippet view article

facies – Cushing's syndrome and polycythemia vera Bird facies – Pierre Robin sequence Ashen grey facies – myocardial infarction Gargoyle facies – Hurler's

SOX9 (2,905 words) [view diff] case mismatch in snippet view article find links to article

transcription unit on either side of SOX9 have been associated with Pierre Robin Sequence, often with a cleft palate. The SOX9 protein has been implicated

Stanislas Lyonnet (884 words) [view diff] exact match in snippet view article find links to article

non-coding elements on either side of the SOX9 gene is associated with Pierre Robin sequence. Nat Genet 2009, 41: 359-64. Putoux A, Thomas S, et al. Costal2

Pharyngeal flap surgery (1,897 words) [view diff] exact match in snippet view article find links to article

been concluded that individuals with Franceschetti syndrome or Pierre Robin sequence are at increased risk for developing airway obstruction following