中文簡(jiǎn)介

美國(guó)醫(yī)學(xué)遺傳學(xué)雜志- A部分(AJMG)為您提供了遺傳疾病和出生缺陷的所有生物學(xué)和醫(yī)學(xué)方面的連續(xù)報(bào)道，以及在當(dāng)前的基因型/表型相關(guān)性背景下的表型分析的深入文檔。除了A部分，AJMG還發(fā)布了另外兩個(gè)部分:第二部分:神經(jīng)精神病學(xué)遺傳學(xué)，包括神經(jīng)和精神疾病的遺傳機(jī)制的實(shí)驗(yàn)和臨床研究。第三部分:醫(yī)學(xué)遺傳學(xué)研討會(huì)，AJMG讀者感興趣的專題評(píng)論的客座編輯合集。作為醫(yī)生、醫(yī)學(xué)遺傳學(xué)家和相關(guān)專業(yè)人士的重要資源，該雜志的主要目的是報(bào)告以下領(lǐng)域的原始研究:生化遺傳學(xué):新生兒篩查、載體檢測(cè)、代謝異常及畸形綜合征;癌癥遺傳學(xué)和癌癥細(xì)胞遺傳學(xué):實(shí)驗(yàn)和分子方法;臨床遺傳學(xué):對(duì)新證候的描述，對(duì)已知證候的新的因果和致病見解，遺傳咨詢、nosology、人體測(cè)量學(xué)和人類學(xué)(包括皮紋學(xué))方面的進(jìn)展;臨床分子遺傳學(xué):連鎖、定位和基因測(cè)序;形式遺傳學(xué):數(shù)量遺傳學(xué)、人口遺傳學(xué)和流行病學(xué)遺傳學(xué);分子細(xì)胞遺傳學(xué):染色體畸變綜合征的描述神經(jīng)精神病學(xué)遺傳學(xué):關(guān)于精神病學(xué)和神經(jīng)系統(tǒng)疾病遺傳機(jī)制的新研究報(bào)告;生殖遺傳學(xué):產(chǎn)前診斷和遺傳學(xué)的產(chǎn)前和圍產(chǎn)期死亡的人。AJMG還報(bào)道了人類遺傳疾病的動(dòng)物模型、倫理、法律和社會(huì)問題、胎兒遺傳病理學(xué)和畸形學(xué)、遺傳漂移、醫(yī)學(xué)遺傳學(xué)的歷史方面以及對(duì)雙胞胎和孿生兒的研究。該雜志通過強(qiáng)調(diào)對(duì)表型和自然歷史條件的詳細(xì)記錄，著重于圍繞仔細(xì)的表型分析的主題。除了研究文章，雜志的常規(guī)特征還包括臨床報(bào)告、社論、快速出版物和給編輯的信件。

投稿網(wǎng)址：https://mc.manuscriptcentral.com/ajmg-a

英文簡(jiǎn)介

The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts:Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders.Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .As a crucial resource to physicians, medical geneticists and associated professionals, the Journal's primary purpose is to report original research in the following areas:Biochemical Genetics : newborn screening, carrier detection, and the metabolic dysplasia and malformation syndromes;Cancer Genetics and Cancer Cytogenetics : experimental and molecular approaches;Clinical Genetics : descriptions of new syndromes, new causal and pathogenetic insights into known syndromes, advances in genetic counseling, nosology, anthropometry, and anthropology, including dermatoglyphics;Clinical Molecular Genetics : linkage, mapping, and gene sequencing;Formal Genetics : quantitative, population, and epidemiological genetics;Molecular Cytogenetics : delineation of syndromes due to chromosomal aberration;Neuropsychiatric Genetics : reports on novel research on the genetic mechanisms underlying psychiatric and neurological disorders;Reproductive Genetics : prenatal diagnosis and the genetics of prenatal and perinatal death in humans.AJMG also reports on animal models of human genetic disorders, ethical, legal and social issues, fetal genetic pathology and teratology, genetic drift, historical aspects of medical genetics, and studies of twins and twinning. The Journal focuses on the themes surrounding careful phenotype analysis by emphasizing meticulous documentation of phenotype and natural history of conditions. In addition to research articles, regular features of the Journal include clinical reports, editorials, rapid publications, and letters to the editor.