[XO-XY 嵌合体的疾病分类位置] - Suppr

Suppr

超能文献

[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

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

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

THE SEX CHROMOSOME ANOMALIES.

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

[XO-XY-Xy mosaicism and Turner's syndrome in an 18-year-old girl].

Ann Genet. 1966 Jun;9(2):86-90.

[Intersexuality in childhood].

Med Klin. 1974 Nov 1;69(44):1779-90.

XO-XY CHROMOSOMAL MOSAICISM AND EXTRAGENITAL STIGMATA OF TURNER'S SYNDROME IN A PHENOTYPIC MALE.

J Clin Endocrinol Metab. 1965 Jan;25:141-5. doi: 10.1210/jcem-25-1-141.

[Monosomy X in mosaicism. II. (XO-XY,XO-XY-XXY,SO-XY-?XXY)].

Bratisl Lek Listy. 1970 Feb;53(2):195-206.

MOSAICISM.

N Engl J Med. 1965 Jan 7;272:34-5. doi: 10.1056/NEJM196501072720108.

[XY/XXY MOSAICISM IN A CHILD WITH MALE GENITAL DYSGENESIS].

Ann Endocrinol (Paris). 1964 Sep-Oct;25:536-43.

The indications for chromosome analysis as an aid to the clinician.

Clin Pediatr (Phila). 1968 Feb;7(2):83-7. doi: 10.1177/000992286800700208.

Genetic studies in cases of abnormal sex determination and differentiation.

Pol Med Sci Hist Bull. 1969 Oct;12(4):168-72.

引用本文的文献

Sex chromosome DSD individuals with mosaic 45,X0 and aberrant Y chromosomes in 46,XY cells: distinct gender phenotypes and germ cell tumour risks.

Syst Biol Reprod Med. 2022 Aug;68(4):247-257. doi: 10.1080/19396368.2022.2057258. Epub 2022 Apr 28.

A case of 46,XY-45,X-46,XX intersex.

Humangenetik. 1971;12(3):244-54. doi: 10.1007/BF00702776.

A phenotypically Turner-like female with karyotype 45,X/46,XY, gonadoblastoma and fluorescent Y.

Humangenetik. 1974;24(4):309-18. doi: 10.1007/BF00297595.

Male pseudohermaphroditism: genetics and clinical delineation.

Hum Genet. 1978 Oct 19;44(1):1-49. doi: 10.1007/BF00283573.

本文引用的文献

[Study of karyotypes in Stein-Leventhal syndrome].

Ann Endocrinol (Paris). 1961 Nov-Dec;22:841-9.

[Male Turnerian pseudohermaphroditism].

Sem Hop. 1962 May 20;38:1699-705.

The sex chromosomes in abnormalities of sexual differentiation.

Am J Med Sci. 1962 Jun;243:790-807. doi: 10.1097/00000441-196206000-00010.

The chromosomes in a case of pure gonadal dysgenesis.

Br Med J. 1959 Dec 12;2(5162):1285-7. doi: 10.1136/bmj.2.5162.1285.

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.

[AN XX/XY-HERMAPHRODITE WITH AN "INTRATUBULAR OVUM" AND A GONADOBLASTOMA (GONOCYTOMA 3)].

Klin Wochenschr. 1964 Nov 1;42:1052-60. doi: 10.1007/BF01486344.

PURE GONADAL DYSGENESIS; REPORT OF A CASE.

Am J Dis Child. 1965 Aug;110:203-5. doi: 10.1001/archpedi.1965.02090030213022.

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.

J Med Genet. 1965 Jun;2(2):142-55. doi: 10.1136/jmg.2.2.142.

MIXED GONADAL DYSGENESIS WITH XX-XY MOSAICISM. THE EVIDENCE FOR THE OCCURRENCE OF FERTILISATION BY TWO SPERMATOZOA IN MAN.

Lancet. 1965 May 15;1(7394):1035-9. doi: 10.1016/s0140-6736(65)91313-9.

TWO XY SIBLINGS WITH GONADAL DYSGENESIS AND A FEMALE PHENOTYPE.

N Engl J Med. 1965 May 27;272:1083-8. doi: 10.1056/NEJM196505272722101.

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

相似文献

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

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

THE SEX CHROMOSOME ANOMALIES.

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

[XO-XY-Xy mosaicism and Turner's syndrome in an 18-year-old girl].

Ann Genet. 1966 Jun;9(2):86-90.

[Intersexuality in childhood].

Med Klin. 1974 Nov 1;69(44):1779-90.

XO-XY CHROMOSOMAL MOSAICISM AND EXTRAGENITAL STIGMATA OF TURNER'S SYNDROME IN A PHENOTYPIC MALE.

J Clin Endocrinol Metab. 1965 Jan;25:141-5. doi: 10.1210/jcem-25-1-141.

[Monosomy X in mosaicism. II. (XO-XY,XO-XY-XXY,SO-XY-?XXY)].

Bratisl Lek Listy. 1970 Feb;53(2):195-206.

MOSAICISM.

N Engl J Med. 1965 Jan 7;272:34-5. doi: 10.1056/NEJM196501072720108.

[XY/XXY MOSAICISM IN A CHILD WITH MALE GENITAL DYSGENESIS].

Ann Endocrinol (Paris). 1964 Sep-Oct;25:536-43.

The indications for chromosome analysis as an aid to the clinician.

Clin Pediatr (Phila). 1968 Feb;7(2):83-7. doi: 10.1177/000992286800700208.

Genetic studies in cases of abnormal sex determination and differentiation.

Pol Med Sci Hist Bull. 1969 Oct;12(4):168-72.

引用本文的文献

Sex chromosome DSD individuals with mosaic 45,X0 and aberrant Y chromosomes in 46,XY cells: distinct gender phenotypes and germ cell tumour risks.

Syst Biol Reprod Med. 2022 Aug;68(4):247-257. doi: 10.1080/19396368.2022.2057258. Epub 2022 Apr 28.

A case of 46,XY-45,X-46,XX intersex.

Humangenetik. 1971;12(3):244-54. doi: 10.1007/BF00702776.

A phenotypically Turner-like female with karyotype 45,X/46,XY, gonadoblastoma and fluorescent Y.

Humangenetik. 1974;24(4):309-18. doi: 10.1007/BF00297595.

Male pseudohermaphroditism: genetics and clinical delineation.

Hum Genet. 1978 Oct 19;44(1):1-49. doi: 10.1007/BF00283573.

本文引用的文献

[Study of karyotypes in Stein-Leventhal syndrome].

Ann Endocrinol (Paris). 1961 Nov-Dec;22:841-9.

[Male Turnerian pseudohermaphroditism].

Sem Hop. 1962 May 20;38:1699-705.

The sex chromosomes in abnormalities of sexual differentiation.

Am J Med Sci. 1962 Jun;243:790-807. doi: 10.1097/00000441-196206000-00010.

The chromosomes in a case of pure gonadal dysgenesis.

Br Med J. 1959 Dec 12;2(5162):1285-7. doi: 10.1136/bmj.2.5162.1285.

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.

[AN XX/XY-HERMAPHRODITE WITH AN "INTRATUBULAR OVUM" AND A GONADOBLASTOMA (GONOCYTOMA 3)].

Klin Wochenschr. 1964 Nov 1;42:1052-60. doi: 10.1007/BF01486344.

PURE GONADAL DYSGENESIS; REPORT OF A CASE.

Am J Dis Child. 1965 Aug;110:203-5. doi: 10.1001/archpedi.1965.02090030213022.

KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS.

J Med Genet. 1965 Jun;2(2):142-55. doi: 10.1136/jmg.2.2.142.

MIXED GONADAL DYSGENESIS WITH XX-XY MOSAICISM. THE EVIDENCE FOR THE OCCURRENCE OF FERTILISATION BY TWO SPERMATOZOA IN MAN.

Lancet. 1965 May 15;1(7394):1035-9. doi: 10.1016/s0140-6736(65)91313-9.

TWO XY SIBLINGS WITH GONADAL DYSGENESIS AND A FEMALE PHENOTYPE.

N Engl J Med. 1965 May 27;272:1083-8. doi: 10.1056/NEJM196505272722101.