A computer based system of coding for genetic studies of large kindreds

Does small mammal prey guild affect the exposure of predators to anticoagulant rodenticides?

Environmental pollution (Barking, Essex : 1987)·2011

HOST FACTORS IN THE PATHOGENESIS OF PNEUMOCOCCUS PNEUMONIA : I. THE REACTION OF THE LUNGS TO PNEUMOCOCCUS AUTOLYSATE IN SENSITIZED RABBITS.

The Journal of experimental medicine·2009

Determination of chloralose residues in animal tissues by liquid chromatography-electrospray ionisation tandem mass spectrometry.

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences·2004

Phenotypic expression of disease in families that have mutations in the 5' region of the adenomatous polyposis coli gene.

Annals of internal medicine·1997

APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis.

Gut·1997

Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposis.

Ophthalmic genetics·1996

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Human heredity·2026

Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

Human heredity·2026

Erratum.

Human heredity·2026

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Human heredity·2025

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

Human heredity·2025

Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size.

Human heredity·2025

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

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A computer based system of coding for genetic studies of large kindreds

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Does small mammal prey guild affect the exposure of predators to anticoagulant rodenticides?

HOST FACTORS IN THE PATHOGENESIS OF PNEUMOCOCCUS PNEUMONIA : I. THE REACTION OF THE LUNGS TO PNEUMOCOCCUS AUTOLYSATE IN SENSITIZED RABBITS.

Determination of chloralose residues in animal tissues by liquid chromatography-electrospray ionisation tandem mass spectrometry.

Phenotypic expression of disease in families that have mutations in the 5' region of the adenomatous polyposis coli gene.

APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis.

Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposis.

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

Erratum.

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

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A computer based system of coding for genetic studies of large kindreds

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