{"title":"男性的翼状胬肉-大肠综合征。两个病例的临床、组织学和细胞遗传学研究。","authors":"K H GUSTAVSON, B HAGBERG, H KNUTSON, S SJOELIN","doi":"10.1111/j.1651-2227.1964.tb07251.x","DOIUrl":null,"url":null,"abstract":"In phenotypical females with gonadal dysgenesis most cases are chromatin negative, with a chromosome number of 45 and an XO sex chromosome constitution. This was the first chromosomal constitution to be described in Turner’s syndrome [9, 101. Some females with gonadal dysgenesis are chromatin positive. Chromosomal analyses in these cases have shown a variety of X-chromosome anomalies, including XOjXX mosaicism, isochromosomes and deletions of the X-chromosome, but a few of them have had a normal female karyotype [5, 17, 221. Women are occasionally seen who have P61.","PeriodicalId":7043,"journal":{"name":"Acta Pædiatrica","volume":" ","pages":"454-64"},"PeriodicalIF":0.0000,"publicationDate":"1964-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1651-2227.1964.tb07251.x","citationCount":"15","resultStr":"{\"title\":\"THE PTERYGIUM-COLLI SYNDROME IN THE MALE. A CLINICAL, HISTOLOGICAL, AND CYTOGENETIC STUDY OF TWO CASES.\",\"authors\":\"K H GUSTAVSON, B HAGBERG, H KNUTSON, S SJOELIN\",\"doi\":\"10.1111/j.1651-2227.1964.tb07251.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In phenotypical females with gonadal dysgenesis most cases are chromatin negative, with a chromosome number of 45 and an XO sex chromosome constitution. This was the first chromosomal constitution to be described in Turner’s syndrome [9, 101. Some females with gonadal dysgenesis are chromatin positive. Chromosomal analyses in these cases have shown a variety of X-chromosome anomalies, including XOjXX mosaicism, isochromosomes and deletions of the X-chromosome, but a few of them have had a normal female karyotype [5, 17, 221. Women are occasionally seen who have P61.\",\"PeriodicalId\":7043,\"journal\":{\"name\":\"Acta Pædiatrica\",\"volume\":\" \",\"pages\":\"454-64\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1964-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1111/j.1651-2227.1964.tb07251.x\",\"citationCount\":\"15\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Pædiatrica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1111/j.1651-2227.1964.tb07251.x\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Pædiatrica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1111/j.1651-2227.1964.tb07251.x","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
THE PTERYGIUM-COLLI SYNDROME IN THE MALE. A CLINICAL, HISTOLOGICAL, AND CYTOGENETIC STUDY OF TWO CASES.
In phenotypical females with gonadal dysgenesis most cases are chromatin negative, with a chromosome number of 45 and an XO sex chromosome constitution. This was the first chromosomal constitution to be described in Turner’s syndrome [9, 101. Some females with gonadal dysgenesis are chromatin positive. Chromosomal analyses in these cases have shown a variety of X-chromosome anomalies, including XOjXX mosaicism, isochromosomes and deletions of the X-chromosome, but a few of them have had a normal female karyotype [5, 17, 221. Women are occasionally seen who have P61.
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
