A Case Report of Camptomelic Dysplasia

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Iranian journal of child neurology

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  DOI 10.22037/IJCN.V5I3.2407
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

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• Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 gene

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• Campomelic dysplasia: a rare cause of congenital spinal deformity.

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• Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9

  2009cited by this paper
• [Camptomelic dysplasia--a case report].

  2007cited by this paper
• Prenatal diagnosis of campomelic dysplasia with three‐dimensional ultrasound

  2006cited by this paper
• Congenital cervical instability in a patient with camptomelic dysplasia

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• Camptomelic dysplasia in Mazandaran, a case report

  2004cited by this paper
• The phenotype of survivors of campomelic dysplasia

  2002cited by this paper
• Campomelic dysplasia in a twin pregnancy. A case report.

  1998cited by this paper
• Campomelic dysplasia associated with mandibular clefting.

  1996cited by this paper
• A clinical and genetic study of campomelic dysplasia.

  1995cited by this paper
• Assignment of an autosomal sex reversa– locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3–q25.1

  1993cited by this paper
• [The campomelic syndrome].

  1971cited by this paper

• No citing papers are available for this paper.