Neural Tube Defects and Chromosome Deletions

J Gordon Millichap

doi:10.15844/pedneurbriefs-10-12-7

Neural Tube Defects and Chromosome Deletions

Pediatric Neurology Briefs

Volume 10 (1996): Issue 12

By: J Gordon Millichap

Open Access

|Dec 1996

Abstract

Patients with neural tube defects (NTDs) complicated by congenital heart defects, facial anomalies, thymic hypoplasia, cleft lip or palate, or hypocalcemia and a family history of NTDs and other anomalies were tested for 22qll deletions at the Departments of Pediatrics and Molecular Genetics, Oregon Health Sciences University, Eugene, Oregon.

References

Nickel RE Magenis RE Neural tube defects and deletions of 22q11 Am J Med Genet 1996 Dec 2 66 1 25 27 10.1002/(SICI)1096-8628(19961202)66:1<;25::AID-AJMG6>3.3.CO;2-A 8957506
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DOI: https://doi.org/10.15844/pedneurbriefs-10-12-7 | Journal eISSN: 2166-6482

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Language: English

Page range: 93 - 93

Published on: Dec 1, 1996

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Neural Tube Defects,

Hypocalcemia,

Conotruncal Defect

© 1996 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 10 (1996): Issue 12