Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma Associated with 9p Deletion Syndrome

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Ophthalmic Genetics

• Publication date

  2007-01-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1080/13816810701351339PMID 17558847
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma with Trisomy 8q22-Qter/ Monosomy 9p23-Pter

  2005cited by this paper
• Congenital glaucoma in a child with partial 1q duplication and 9p deletion.

  1992cited by this paper
• Eleven new cases of del(9p) and features from 80 cases.

  1988cited by this paper
• Primary congenital glaucoma in a patient with trisomy 2q (q33----qter) and monosomy 9p(p24----pter). Case report.

  1987cited by this paper
• Congenital glaucoma and other ocular abnormalities associated with pericentric inversion of chromosome 11.

  1983cited by this paper
• Pericentric inversions of chromosome 9 in two families.

  1972cited by this paper
• Recognizable Patterns of Human Malformation. Genetic, Embryologic and Clinical Aspects

  1971cited by this paper
• Recognizable patterns of human malformation: genetic, embryologic, and clinical aspects.

  1970cited by this paper

• A case of 9p deletion syndrome with congenital infantile glaucoma, effective method of diagnosis, and treatment.

  2017cites this paper
• Oculofacial Manifestations of Chromosomal Aberrations

  2017cites this paper
• Clinical classification of childhood glaucomas.

  2010cites this paper