"mendelian randomization" trang 2 - tải miễn phí từ tailieuXANH
Báo cáo y học:

Báo cáo y học: ": Unlocking Mendelian disease using exome sequencing"
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Báo cáo y học:

Báo cáo y học: "Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes"
9    56    0
Lecture Biology: Chapter 14 - Niel Campbell, Jane Reece

Lecture Biology: Chapter 14 - Niel Campbell, Jane Reece
69    52    1
Lecture Genetics: From genes to genomes - Chapter 14: Prokaryotic and organelle genetics

Lecture Genetics: From genes to genomes - Chapter 14: Prokaryotic and organelle genetics
69    73    1
Ebook BRS Genetics: Part 1

Ebook BRS Genetics: Part 1
109    73    3
Ebook Medical genetics at a glance (3rd edition): Part 1

Ebook Medical genetics at a glance (3rd edition): Part 1
107    49    0
Lecture Biology 25 (Human Biology): Chapter 19, 20 - Prof. Gonsalves

Lecture Biology 25 (Human Biology): Chapter 19, 20 - Prof. Gonsalves
89    78    0
Lecture AP Biology - Chapter 14: Mendel and the gene idea

Lecture AP Biology - Chapter 14: Mendel and the gene idea
36    85    1
Diferential gene regulatory pattern in the human brain from schizophrenia using transcriptomic‑causal network

Diferential gene regulatory pattern in the human brain from schizophrenia using transcriptomic‑causal network
19    57    0
SLMSuite: A suite of algorithms for segmenting genomic profiles

SLMSuite: A suite of algorithms for segmenting genomic profiles
5    69    0
Gentrepid V2.0: A web server for candidate disease gene prediction

Gentrepid V2.0: A web server for candidate disease gene prediction
9    61    0
A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease

A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease
10    40    1
Association of a rare NOTCH4 coding variant with systemic sclerosis: A family-based whole exome sequencing study

Association of a rare NOTCH4 coding variant with systemic sclerosis: A family-based whole exome sequencing study
6    40    1
Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants

Cruxome: A powerful tool for annotating, interpreting and reporting genetic variants
9    31    1
Risk-modeling of dog osteosarcoma genome scans shows individuals with Mendelian-level polygenic risk are common

Risk-modeling of dog osteosarcoma genome scans shows individuals with Mendelian-level polygenic risk are common
14    218    1
Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics

Genome analysis and pleiotropy assessment using causal networks with loss of function mutation and metabolomics
16    59    1
Lecture Essentials of Genetics

Lecture Essentials of Genetics
351    236    1
Blood lipids influence DNA methylation in circulating cells

Blood lipids influence DNA methylation in circulating cells
12    18    1
GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition

GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition
9    68    1
A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)- creating mutation

A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)- creating mutation
10    126    1
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