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1
Comments on patients with sex chromosome aneuploidy: dermatoglyphs, parental ages, Xg a blood group.性染色体非整倍体患者的相关评论:皮纹、父母年龄、Xg血型
J Med Genet. 1970 Dec;7(4):345-50. doi: 10.1136/jmg.7.4.345.
2
Dermatoglyphs in sex chromosome anomalies.
J Ment Defic Res. 1979 Jun;23(2):91-104. doi: 10.1111/j.1365-2788.1979.tb00046.x.
3
The Xg blood groups and sex-chromosome aneuploidy.Xg血型与性染色体非整倍体
Philos Trans R Soc Lond B Biol Sci. 1970 Aug 6;259(828):37-40. doi: 10.1098/rstb.1970.0043.
4
Xg and sex-chromosome abnormalities.Xg与性染色体异常。
Br Med Bull. 1969 Jan;25(1):99-103. doi: 10.1093/oxfordjournals.bmb.a070677.
5
[Dermatoglyphics in medical genetics].
Rev Paul Med. 1968 Apr;72(4):173-204.
6
Xg groups and sex abnormalities in people of northern European ancestry.北欧血统人群中的Xg血型组与性异常
J Med Genet. 1971 Dec;8(4):417-26. doi: 10.1136/jmg.8.4.417.
7
Origin of sex chromosome monosomy in man.人类性染色体单体性的起源
J Med Genet. 1971 Dec;8(4):501-3. doi: 10.1136/jmg.8.4.501.
8
Dosage of Sex Chromosomal Genes in Blood Deposited on Filter Paper for Neonatal Screening of Sex Chromosome Aneuploidy.用于新生儿性染色体非整倍体筛查的滤纸上血样中性染色体基因的剂量
Genet Test Mol Biomarkers. 2016 Dec;20(12):786-790. doi: 10.1089/gtmb.2016.0101. Epub 2016 Oct 19.
9
On the origin of 46,XX and 47,XXY males, 46,XY females and the position of the Xg locus.关于46,XX和47,XXY男性的起源、46,XY女性以及Xg基因座的位置
Ann Hum Genet. 1973 Jul;37(1):21-30. doi: 10.1111/j.1469-1809.1973.tb01811.x.
10
Sex chromosome aneuploidy: the Denver Prospective Study.性染色体非整倍体:丹佛前瞻性研究
Birth Defects Orig Artic Ser. 1990;26(4):59-115.

引用本文的文献

1
Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY.多种X和Y染色体疾病中的社会功能:XXY、XYY、XXYY、XXXY。
Dev Disabil Res Rev. 2009;15(4):328-32. doi: 10.1002/ddrr.76.
2
The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.失活染色体对人类发育的影响。异常性染色体组成与表型。
Humangenetik. 1973;17(2):105-36. doi: 10.1007/BF00277906.
3
[XXXY Klinefelter's syndrome].
Humangenetik. 1972;15(4):327-33. doi: 10.1007/BF00281732.
4
Klinefelter's syndrome in Sardinia and Scotland. Comparative studies of parental age and other aetiological factors in 47,XXY.撒丁岛和苏格兰的克兰费尔特综合征。47,XXY患者父母年龄及其他病因学因素的比较研究。
Hum Genet. 1988 Dec;81(1):71-5. doi: 10.1007/BF00283733.
5
X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.一名智力发育迟缓男性的X-Y易位。临床、细胞遗传学、生物化学及血清遗传学研究。
J Med Genet. 1978 Dec;15(6):466-74. doi: 10.1136/jmg.15.6.466.

本文引用的文献

1
SUCCESSIVE NON-DISJUNCTION AT FIRST AND SECOND MEIOTIC DIVISION OF SPERMATOGENESIS: EVIDENCE OF CHROMOSOMES AND XG.精子发生过程中第一次和第二次减数分裂的连续不分离:染色体和XG的证据
Cytogenetics. 1964;3:334-41. doi: 10.1159/000129822.
2
DERMATOGLYPHIC ANOMALIES IN TURNER'S SYNDROME.特纳综合征的皮纹异常
Ann Hum Genet. 1964 Sep;28:87-100. doi: 10.1111/j.1469-1809.1964.tb00463.x.
3
DERMATOGLYPHICS ASSOCIATED WITH THE XXYH CHROMOSOME COMPLEMENT.与XXY染色体组型相关的肤纹学
Am J Hum Genet. 1964 Sep;16(3):284-91.
4
FINGERPRINTS AND PALM PRINTS (DERMATOGLYPHICS) AND PALMAR-FLEXION CREASES IN GONADAL DYSGENESIS, PSEUDOHYPOPARATHYROIDISM AND KLINEFELTER'S SYNDROME.性腺发育不全、假性甲状旁腺功能减退症及克兰费尔特综合征中的指纹、掌纹(皮纹学)及掌屈褶纹
N Engl J Med. 1964 Jun 11;270:1268-77. doi: 10.1056/NEJM196406112702402.
5
Parental origin of the sex chromosomes in the XO and XXY karyotypes in man.人类XO和XXY核型中性染色体的亲本来源。
Ann Hum Genet. 1963 Jun;26:297-304. doi: 10.1111/j.1469-1809.1963.tb01325.x.
6
Primary amentia and micro-orchidism associated with an XXXY sex-chromosome constitution.原发性智力缺陷和小睾丸症与XXXY性染色体构成相关。
Lancet. 1960 Jul 23;2(7143):184-7. doi: 10.1016/s0140-6736(60)91329-5.
7
The use of dermal configurations in the diagnosis of mongolism.皮肤形态在先天愚型诊断中的应用。
Pediatr Clin North Am. 1958 May:531-43. doi: 10.1016/s0031-3955(16)30666-6.
8
Dermatoglyphics in XXYY Klinefelter's syndrome.XXYY克氏综合征中的皮纹学。
Am J Hum Genet. 1966 Nov;18(6):507-13.
9
Is hyperploidy of sex chromosomes associated with reduced total finger ridge count?性染色体超倍体与总指嵴数减少有关吗?
Am J Hum Genet. 1965 Nov;17(6):473-5.
10
Dermatoglyphics of the XYY Syndrome.
Am J Phys Anthropol. 1969 Mar;30(2):209-13. doi: 10.1002/ajpa.1330300207.

Comments on patients with sex chromosome aneuploidy: dermatoglyphs, parental ages, Xg a blood group.

作者信息

Borgaonkar D S, Mules E

出版信息

J Med Genet. 1970 Dec;7(4):345-50. doi: 10.1136/jmg.7.4.345.

DOI:10.1136/jmg.7.4.345
PMID:5503472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468944/
Abstract
摘要