## Abstract A patient with partial deletion of the long arm of chromosome 11[del(11)(q23.3→qter)] had macrocephalic trigonocephaly, growth and mental retardation, congenital heart defect, and characteristic facial appearance familiar to that of 33 other reported patients with this deletion. Compute
Assignment of the apolipoprotein A-I gene to 11q23 based on RFLP in a case with a partial deletion of chromosome 11, del(11)(q23.3→qter)
✍ Scribed by Tadao Arinami; Takeki Hirano; Kimiko Kobayashi; Yasuko Yamanouchi; Hideo Hamaguchi
- Publisher
- Springer
- Year
- 1990
- Tongue
- English
- Weight
- 246 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0340-6717
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✦ Synopsis
The XmnI genotype at the apolipoprotein A-I locus was heterozygous in a boy with partial deletion of the long arm of chromosome 11, del(11)(q23.3----qter). The apolipoprotein A-I gene, previously assigned to chromosome region 11q23----q24, has been more specifically localized to 11q23 by excluding the region 11q24----qter.
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