多功能互动图形显示系统用于计算机分子建模.

Same author

The incremental risk of fragility fractures in aging men.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2023

Same author

De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.

Clinical genetics·2017

Same author

Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance.

Clinical genetics·2017

Same author

Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features.

Clinical genetics·2016

Same author

Paradoxical worsening of pemphigus vulgaris following rituximab therapy.

The British journal of dermatology·2015

Same author

Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life.

Clinical genetics·2014

Same journal

Incoming US science academy chief vows to 'double down' on research.

Nature·2026

Same journal

Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

Nature·2026

Same journal

Electrodeposited self-assembled molecules for perovskite photovoltaics.

Nature·2026

Same journal

Neutrino's nursery found: the 'Shadow Blaster'.

Nature·2026

Same journal

Dementia risk in middle-aged people linked to a blood protein.

Nature·2026

Same journal

Daily briefing: What's really happening with trust in science.

Nature·2026

相关实验视频

多功能互动图形显示系统用于计算机分子建模.

相关概念视频

The incremental risk of fragility fractures in aging men.

De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.

Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance.

Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features.

Paradoxical worsening of pemphigus vulgaris following rituximab therapy.

Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life.

Incoming US science academy chief vows to 'double down' on research.

Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

Electrodeposited self-assembled molecules for perovskite photovoltaics.

Neutrino's nursery found: the 'Shadow Blaster'.

Dementia risk in middle-aged people linked to a blood protein.

Daily briefing: What's really happening with trust in science.

相关实验视频

多功能互动图形显示系统用于计算机分子建模.

相关概念视频

相关文章

The incremental risk of fragility fractures in aging men.

De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.

Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance.

Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features.

Paradoxical worsening of pemphigus vulgaris following rituximab therapy.

Depression among adults with neurofibromatosis type 1: prevalence and impact on quality of life.

Incoming US science academy chief vows to 'double down' on research.

Author Correction: Synthesis of enantioenriched atropisomers by biocatalytic deracemization.

Electrodeposited self-assembled molecules for perovskite photovoltaics.

Neutrino's nursery found: the 'Shadow Blaster'.

Dementia risk in middle-aged people linked to a blood protein.

Daily briefing: What's really happening with trust in science.