A case with inv(9)(p11q13).
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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Sawano Kunihiko
Department Of Pediatrics Hiroshima Prefectural Rehabilitation Center
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Watanabe Yoko
The Kadotani Med. Res. Found
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MATSUO Nami
The Kadotani Medical Research Foundation
関連論文
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- A chromosomal study on 22 cases of congenital neural tube defects
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- A case of reciprocal translocation (3p;11q) and inversion (3p)(Abstracts of the 48th Annual Meeting of the Society of Chromosome Research)
- THERMOGRAPHIC FINDINGS OF INFANTS WITH CEREBRAL PALSY
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- Chromosomal fragile sites in the parents and their babies
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- A chromosome study of the patients with heavy mental retardation.
- A case of partial monosomy for the long arm of the no. 9 chromosome.
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- Further Cytogenetic Studies on 105 Cases from Genetic Counseling
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- A case of slight anemia with the long arm interstitial deletion of No. 5 chromosome (46, XY, 5q-).
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- A case of partial monosomy for the short arm of the chromosome No. 9.
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- Fragile sites in newborns.
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- Partial Trisomy 3q22 Involving the No. 15 Short Arm without Association with Cornelia de Lange Syndrome
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- A chromosome study on the 91 cases of the mentally retarded men.
- An 18p- Case with Severe lower Abdominal Deformities
- A case of the Prader-Willi syndrome having the interstitial deletion of No. 15 chromosome.
- A case of X/XX/Xr(X) derived from the father with the chromosome aberrations.
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- A chromosome study of a patient with Wilms' tumor.
- A case with inv(9)(p11q13).
- A case of 1qh+, t(3;4)(q23;p14).
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