日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Origins of human genetics. A personal perspective

人类遗传学的起源:个人视角

Passarge, Eberhard

The early years of the ESHG leading to the reform of 1988 and the spirit of the Sestri Levante school

ESHG的早期发展历程,直至1988年的改革以及塞斯特里莱万特学校的精神

Romeo, Giovanni; Passarge, Eberhard; de la Chapelle, Albert

Marfanoid-progeroid-lipodystrophy syndrome: a newly recognized fibrillinopathy

马凡氏综合征-早衰症-脂肪营养不良综合征:一种新发现的纤维蛋白病

Passarge, Eberhard; Robinson, Peter N; Graul-Neumann, Luitgard M

Improved prediction of complex diseases by common genetic markers: state of the art and further perspectives

利用常见遗传标记改进复杂疾病的预测:现状与展望

Müller, Bent; Wilcke, Arndt; Boulesteix, Anne-Laure; Brauer, Jens; Passarge, Eberhard; Boltze, Johannes; Kirsten, Holger

Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs

通过高分辨率显带和荧光原位杂交(FISH)分析涉及3q、6q和15q染色体的家族性三向易位,结果显示同胞之间存在两种不同的不平衡核型。

Wieczorek, D; Engels, H; Viersbach, R; Henke, B; Schwanitz, G; Passarge, E

Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma

孤立性单侧视网膜母细胞瘤患者的RB1基因突变

Lohmann, D R; Gerick, M; Brandt, B; Oelschläger, U; Lorenz, B; Passarge, E; Horsthemke, B

Microcephalic osteodysplastic primordial dwarfism type I/III in sibs

同胞中患有小头畸形骨发育不良原始侏儒症 I/III 型

Meinecke, P; Passarge, E

Trisomy 8 restricted to cultured fibroblasts

8号染色体三体仅限于培养的成纤维细胞

Niss, R; Passarge, E

Alpha1-antitrypsin phenotypes in sex chromosome mosaicism

性染色体嵌合体中的α1-抗胰蛋白酶表型

Kueppers, F; O'Brien, P; Passarge, E; Rüdiger, H W