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[The nosologic place of the XO-XY mosaicism].

作者信息

Pfeiffer R A, Lambertz B, Friederiszick F K, Distel H, Pawlowitzki I H, Nicole R, Ober K G, Ruckes J

出版信息

Arch Gynakol. 1968;206(4):369-410. doi: 10.1007/BF00668069.

DOI:10.1007/BF00668069
PMID:4893320
Abstract
摘要

相似文献

1
[The nosologic place of the XO-XY mosaicism].[XO-XY 嵌合体的疾病分类位置]
Arch Gynakol. 1968;206(4):369-410. doi: 10.1007/BF00668069.
2
THE SEX CHROMOSOME ANOMALIES.性染色体异常
Am J Obstet Gynecol. 1964 Dec 1;90:SUPPL:1078-139. doi: 10.1016/0002-9378(64)90836-1.
3
[XO-XY-Xy mosaicism and Turner's syndrome in an 18-year-old girl].
Ann Genet. 1966 Jun;9(2):86-90.
4
[Intersexuality in childhood].
Med Klin. 1974 Nov 1;69(44):1779-90.
5
XO-XY CHROMOSOMAL MOSAICISM AND EXTRAGENITAL STIGMATA OF TURNER'S SYNDROME IN A PHENOTYPIC MALE.一名表型男性中的特纳综合征的XO-XY染色体嵌合现象及生殖器外体征
J Clin Endocrinol Metab. 1965 Jan;25:141-5. doi: 10.1210/jcem-25-1-141.
6
[Monosomy X in mosaicism. II. (XO-XY,XO-XY-XXY,SO-XY-?XXY)].
Bratisl Lek Listy. 1970 Feb;53(2):195-206.
7
MOSAICISM.镶嵌性
N Engl J Med. 1965 Jan 7;272:34-5. doi: 10.1056/NEJM196501072720108.
8
[XY/XXY MOSAICISM IN A CHILD WITH MALE GENITAL DYSGENESIS].[一名患有男性生殖器发育不全儿童的XY/XXY嵌合体现象]
Ann Endocrinol (Paris). 1964 Sep-Oct;25:536-43.
9
The indications for chromosome analysis as an aid to the clinician.染色体分析作为临床辅助手段的适应证。
Clin Pediatr (Phila). 1968 Feb;7(2):83-7. doi: 10.1177/000992286800700208.
10
Genetic studies in cases of abnormal sex determination and differentiation.性发育异常病例的遗传学研究。
Pol Med Sci Hist Bull. 1969 Oct;12(4):168-72.

引用本文的文献

1
Sex chromosome DSD individuals with mosaic 45,X0 and aberrant Y chromosomes in 46,XY cells: distinct gender phenotypes and germ cell tumour risks.性染色体 DSD 个体中存在嵌合 45,X0 和异常 Y 染色体的 46,XY 细胞:不同的性别表型和生殖细胞肿瘤风险。
Syst Biol Reprod Med. 2022 Aug;68(4):247-257. doi: 10.1080/19396368.2022.2057258. Epub 2022 Apr 28.
2
A case of 46,XY-45,X-46,XX intersex.一例46,XY-45,X-46,XX两性畸形病例。
Humangenetik. 1971;12(3):244-54. doi: 10.1007/BF00702776.
3
A phenotypically Turner-like female with karyotype 45,X/46,XY, gonadoblastoma and fluorescent Y.

本文引用的文献

1
[Study of karyotypes in Stein-Leventhal syndrome].[ Stein-Leventhal综合征的核型研究]
Ann Endocrinol (Paris). 1961 Nov-Dec;22:841-9.
2
[Male Turnerian pseudohermaphroditism].
Sem Hop. 1962 May 20;38:1699-705.
3
The sex chromosomes in abnormalities of sexual differentiation.
Am J Med Sci. 1962 Jun;243:790-807. doi: 10.1097/00000441-196206000-00010.
4
The chromosomes in a case of pure gonadal dysgenesis.
Humangenetik. 1974;24(4):309-18. doi: 10.1007/BF00297595.
4
Male pseudohermaphroditism: genetics and clinical delineation.男性假两性畸形:遗传学与临床描述
Hum Genet. 1978 Oct 19;44(1):1-49. doi: 10.1007/BF00283573.
一例单纯性腺发育不全患者的染色体
Br Med J. 1959 Dec 12;2(5162):1285-7. doi: 10.1136/bmj.2.5162.1285.
5
IDENTIFICATION OF THE ORIGIN OF THE X CHROMOSOME(S) IN SEX CHROMOSOME ANEUPLOIDY.
Can J Genet Cytol. 1965 Jun;7:214-22. doi: 10.1139/g65-030.
6
[AN XX/XY-HERMAPHRODITE WITH AN "INTRATUBULAR OVUM" AND A GONADOBLASTOMA (GONOCYTOMA 3)].[一名具有“管内卵子”和性腺母细胞瘤(生殖母细胞瘤3型)的XX/XY两性畸形患者]
Klin Wochenschr. 1964 Nov 1;42:1052-60. doi: 10.1007/BF01486344.
7
PURE GONADAL DYSGENESIS; REPORT OF A CASE.
Am J Dis Child. 1965 Aug;110:203-5. doi: 10.1001/archpedi.1965.02090030213022.
8
KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.性腺发育不全中的核型-表型相关性及其对畸形发病机制的影响
J Med Genet. 1965 Jun;2(2):142-55. doi: 10.1136/jmg.2.2.142.
9
MIXED GONADAL DYSGENESIS WITH XX-XY MOSAICISM. THE EVIDENCE FOR THE OCCURRENCE OF FERTILISATION BY TWO SPERMATOZOA IN MAN.伴有XX-XY嵌合体的混合性性腺发育不全。关于人类中两个精子受精发生的证据。
Lancet. 1965 May 15;1(7394):1035-9. doi: 10.1016/s0140-6736(65)91313-9.
10
TWO XY SIBLINGS WITH GONADAL DYSGENESIS AND A FEMALE PHENOTYPE.两名患有性腺发育不全且表现为女性 phenotype 的 XY 同胞。
N Engl J Med. 1965 May 27;272:1083-8. doi: 10.1056/NEJM196505272722101.