A statistical segregation analysis of (21q22q)-translocations

Fatal hyperammonemia after renal transplant due to late-onset urea cycle deficiency: a case report.

Transplantation proceedings·2010

Experiences with risk estimates for carriers of chromosomal reciprocal translocations.

Clinical genetics·1992

Comments on estimations of risks to translocation carriers.

American journal of medical genetics·1989

The incomplete, multiple ascertainment model: assumptions, applications, and alternative models.

Genetic epidemiology·1989

A reanalysis of the New York State prenatal diagnosis data on Down's syndrome and paternal age effects.

Human genetics·1987

Comments on methods and results in: Sherman et al., "Segregation analysis of balanced pericentric inversions in pedigree data".

Clinical genetics·1986

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

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Frontiers in genetics·2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Frontiers in genetics·2026

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Developmental biology·2026

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Journal of neural transmission (Vienna, Austria : 1996)·2026

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

The Plant journal : for cell and molecular biology·2026

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

The Journal of infectious diseases·2026

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A statistical segregation analysis of (21q22q)-translocations

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Fatal hyperammonemia after renal transplant due to late-onset urea cycle deficiency: a case report.

Experiences with risk estimates for carriers of chromosomal reciprocal translocations.

Comments on estimations of risks to translocation carriers.

The incomplete, multiple ascertainment model: assumptions, applications, and alternative models.

A reanalysis of the New York State prenatal diagnosis data on Down's syndrome and paternal age effects.

Comments on methods and results in: Sherman et al., "Segregation analysis of balanced pericentric inversions in pedigree data".

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.

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Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

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A statistical segregation analysis of (21q22q)-translocations

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