Results 1 -
9
of
9
for
Robin sequence
- Pierre Robin sequence is a set of abnormalities affecting the head and face, consisting of a small lower jaw (micrognathia), a tongue that is placed further ...
- ... SOX9 gene cause some cases of isolated Pierre Robin sequence. Individuals with this condition have a small lower ... mouth (a cleft palate). These cases of Pierre Robin sequence are described as isolated because they occur without ...
- ... cancer and developmental disorders such as isolated Pierre Robin sequence . This condition is caused by changes in regions ... particular genes. The enhancers altered in isolated Pierre-Robin sequence control the activity of the SOX9 gene. In ...
- ... A particular group of physical features, called Pierre Robin sequence, is common in people with campomelic dysplasia. Pierre Robin sequence includes an opening in the roof of the ...
- ... A particular group of physical features called Pierre Robin sequence is also common in people with Stickler syndrome. Pierre Robin sequence includes an opening in the roof of the ...
- ... OSMED Heterozygous otospondylomegaepiphyseal dysplasia Otospondylomegaepiphyseal dysplasia, autosomal dominant Pierre Robin syndrome with fetal chondrodysplasia WZS Genetic Testing Registry: Otospondylomegaepiphyseal ...
- ... Rossier J, Personnaz L, Creau N, Blehaut H, Robin S, Delabar JM, Potier MC. ... SE. Chromosome 21: from sequence to applications. Curr Opin Genet Dev. 2001 Jun; ...
- ... or Free article on PubMed Central Schafer IA, Robin NH, ... EM. The DNA sequence and comparative analysis of human chromosome 5. Nature. ...
- ... with 22q11.2 deletion syndrome are missing a sequence of about 3 million DNA building blocks ... Central Robin NH, Shprintzen RJ. Defining the clinical spectrum of ...