Two siblings with the XY-female having heavy mental retardation from the parent with the normal phenotype.
スポンサーリンク
概要
著者
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Kadotani Tetsuji
The Kadotani Med. Res. Found
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Watanabe Yoko
The Kadotani Med. Res. Found
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TAKEMURA Ichiro
Kojika Educational and Medical Research Foundation
関連論文
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- A chromosomal study on 61 cases with mental retardation.
- An additional case of partial trisomy for the No. 15 chromosome.
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- A chromosome study of the patients with heavy mental retardation.
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- A chromosomal study on the 56 cases of cerebral palsy.
- A study of the fragile sites in the cases with ring chromosome No. 22.
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- A chromosomal study on 121 cases with heavy mental retardation.
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- Chromosome studies on four patients with Alzheimer's disease.
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- A Case of Partial Trisomy 22 without Cat-Eye Stigmata
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- A case of a female infant with terminal deletion of the long arm of No. 4 chromosome.
- A case of partial trisomy 4q resulting from familial (4;9)(q23;p24) translocation.
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- A case of slight anemia with the long arm interstitial deletion of No. 5 chromosome (46, XY, 5q-).
- A case of partial 9q trisomy.
- A case of partial monosomy for the short arm of the chromosome No. 9.
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- A chromosome study of the congenital defectives and their relatives seeking genetic advices.
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- Two siblings with the XY-female having heavy mental retardation from the parent with the normal phenotype.
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- Fragile sites in newborns.
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- A case of X/XX/Xr(X) derived from the father with the chromosome aberrations.
- A chromosome study on the 751 cases of the congenital defectives and their relatives.
- A chromosome study of a patient with Wilms' tumor.
- A case with inv(9)(p11q13).
- A case of 1qh+, t(3;4)(q23;p14).
- The fragile sites in chromosomes on a case with Prader-Willi syndrome.