唐氏综合征（先天愚型）的细胞遗传学。一、一系列因遗传咨询和诊断前来就诊患者的数据。 - Suppr

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

作者信息

HAMERTON J L, GIANNELLI F, POLANI P E

出版信息

Cytogenetics. 1965;4:171-85. doi: 10.1159/000129853.

DOI:10.1159/000129853

PMID:14332559

Abstract

摘要

相似文献

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

Cytogenetics. 1965;4:171-85. doi: 10.1159/000129853.

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). II. THE FREQUENCY OF INTERCHANGE TRISOMY IN PATIENTS BORN AT A MATERNAL AGE OF LESS THAN 30 YEARS.

Cytogenetics. 1965;4:186-92. doi: 10.1159/000129854.

THE CHROMOSOMES--AN INTRODUCTION--WITH SOME OBSERVATIONS IN INDIAN CHILDREN.

Indian J Pediatr. 1964 Jun;31:175-86. doi: 10.1007/BF02803817.

CHROMOSOMES WITHOUT TEARS. I.

Practitioner. 1964 Jul;193:61-8 CONTD.

AUTOSOMAL AND SEX CHROMOSOMAL ANEUPLOIDY: AN EXHIBIT.

J Iowa Med Soc. 1963 Nov;53:735-52.

[Significance of chromosomal mosaicism in clinical diagnosis and genetic counseling].

Cesk Pediatr. 1970 Sep;25(9):435-8.

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). 3. FREQUENCY OF INTERCHANGE OF TRISOMICS AND MUTATION RATE OF CHROMOSOME INTERCHANGES.

Cytogenetics. 1965;4:193-206. doi: 10.1159/000129855.

THE SEX CHROMOSOME ANOMALIES.

Am J Obstet Gynecol. 1964 Dec 1;90:SUPPL:1078-139. doi: 10.1016/0002-9378(64)90836-1.

SEX CHROMATIN.

J Med Genet. 1964 Sep;1(1):50-76. doi: 10.1136/jmg.1.1.50.

MATERNAL MOSAICISM AND DOWN'S SYNDROME (MONGOLISM).

J Pediatr. 1963 Oct;63:599-604. doi: 10.1016/s0022-3476(63)80370-4.

引用本文的文献

The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues.

Am J Med Genet A. 2009 Feb 15;149A(4):573-83. doi: 10.1002/ajmg.a.32729.

Evidence for methylation of inactive human rRNA genes in amplified regions.

Hum Genet. 1981;56(3):315-20. doi: 10.1007/BF00274686.

Trisomy 21q: 46,XX,21s+/47,XX,+21q-(q22----qter) mosaicism (de novo) in a Down syndrome child.

Indian J Pediatr. 1984 May-Jun;51(410):363-6. doi: 10.1007/BF02754689.

A sex chromatin survey of newborn children in two London hospitals.

J Med Genet. 1967 Dec;4(4):258-9. doi: 10.1136/jmg.4.4.258.

[To the genetics and clinical aspects of small chromosome aberrations. A chromosome Gp-h and a chromosome Gs- in one family].

Humangenetik. 1968;5(2):107-18. doi: 10.1007/BF00278671.

Double satellites: autoradiographic study of a chromosomal marker observed in two generations.

Humangenetik. 1971;14(1):6-12. doi: 10.1007/BF00273026.

Frequency of satellite association in individuals with structural abnormalities of nucleolus organiser region.

Humangenetik. 1973 Apr 16;18(2):111-5. doi: 10.1007/BF00291477.

Down's syndrome. Current stage of cytogenetic research.

Humangenetik. 1971;12(1):1-28. doi: 10.1007/BF00291028.

[Chromosome findings in 365 patients with Down's syndrome or suspected Down's syndrome].

Humangenetik. 1970;8(4):307-11. doi: 10.1007/BF00280329.

Short arm enlargement in acrocentric chromosomes.

Am J Hum Genet. 1969 May;21(3):293-304.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

作者信息

出版信息

相似文献

引用本文的文献

文献AI研究员

用中文搜PubMed

文档翻译

Suppr 超能文献

相似文献

引用本文的文献