ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER.
作者信息
DELACHAPELLE A, AULA P, KIVALO E
出版信息
Cytogenetics. 1963;2:129-39. doi: 10.1159/000129774.
PMID:14099757
Abstract
摘要
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ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER.
Cytogenetics. 1963;2:129-39. doi: 10.1159/000129774.
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Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.与触珠蛋白或过氧化氢酶活性丧失无关的D1染色体短臂家族性缺失（46, XX, 13 p-）
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The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.手-足-子宫综合征：一种以手足发育异常、皮纹异常及女性生殖道部分重复为特征的新型遗传性疾病。
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Screening the neonate for development and genetic disorders.
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引用本文的文献
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Familial occurrence of trisomy 22.22三体综合征的家族性发生情况。
Am J Hum Genet. 1968 Mar;20(2):107-18.
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A family with an inherited marker chromosome (46,D-,mar15+).一个具有遗传性标记染色体（46，D-，mar15+）的家族。
Am J Hum Genet. 1971 May;23(3):281-8.
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A marker chromosome number 14 with double satellite obseved in two generations: an unbalanced chromosome constitution associated with normal phenotype.在两代人中观察到一条带有双随体的标记染色体14：一种与正常表型相关的染色体不平衡构成。
Humangenetik. 1972;15(2):191-5. doi: 10.1007/BF00295748.
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[Enlargement of the short arm region of a small acrocentric chromosome].[一条小近端着丝粒染色体短臂区域的增大]
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Short arm enlargement in acrocentric chromosomes.近端着丝粒染色体短臂增大。
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Morphological variability of the human chromosomes in two Indian populations - Rajputs and Punjabis.两个印度人群体——拉杰普特人和旁遮普人中人类染色体的形态变异
Humangenetik. 1975 Aug 29;29(1):67-78. doi: 10.1007/BF00273352.
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