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Results 1 - 9 of 9 for Robin sequence
  1. 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 ...
  2. ... 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 ...
  3. ... 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 ...
  4. ... 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 ...
  5. ... 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 ...
  6. ... OSMED Heterozygous otospondylomegaepiphyseal dysplasia Otospondylomegaepiphyseal dysplasia, autosomal dominant Pierre Robin syndrome with fetal chondrodysplasia WZS Genetic Testing Registry: Otospondylomegaepiphyseal ...
  7. ... 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; ...
  8. ... or Free article on PubMed Central Schafer IA, Robin NH, ... EM. The DNA sequence and comparative analysis of human chromosome 5. Nature. ...
  9. ... 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 ...