NIHのイントラミュラルプログラムです.

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

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

Clinical genetics·2014

Same author

The role of trial tracking on rats' successive delayed matching-to-sample modality performance.

Behavioural processes·2014

関連する実験動画

NIHのイントラミュラルプログラムです.

関連する概念動画

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.

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

The role of trial tracking on rats' successive delayed matching-to-sample modality performance.

関連する実験動画

NIHのイントラミュラルプログラムです.

関連する概念動画

関連記事

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.

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

The role of trial tracking on rats' successive delayed matching-to-sample modality performance.