Reply to a response by Sherman & Iselius to comments on the segregation of balanced pericentric inversions

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

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Experiences with risk estimates for carriers of chromosomal reciprocal translocations.

Clinical genetics·1992

Comments on estimations of risks to translocation carriers.

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

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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".

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Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

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Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

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Avl9 defines a family of DENN domain GTPase-activating proteins.

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Identification of Critical Genes for Recurrent Aphthous Ulcer by Transcriptome Data Analysis and Mendelian Randomization.

Oral health & preventive dentistry·2026

CD71-based immature RBC (iRBC) analysis in peripheral blood has a better correlation with leukocyte PNH clone size and improves the delineation of different PNH clone types.

Cytometry. Part B, Clinical cytometry·2026

Costello Syndrome Associated With Somatic Mosaicism of Rare p.Gly13Asp HRAS Variant: Expanding the Phenotypic Spectrum.

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A novel prognostic model based on Golgi apparatus-related genes predicts patient survival in glioblastoma.

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Related Experiment Videos

Reply to a response by Sherman & Iselius to comments on the segregation of balanced pericentric inversions

Related Concept Videos

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".

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

Biallelic ABCA13 Loss-of-Function Variants in a Child With Neurodevelopmental Delay: A Case Report.

Variants in the Imprinted IGF2 Gene: A Review and Phasing of De Novo Variants Using Long-Read Sequencing.

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Avl9 defines a family of DENN domain GTPase-activating proteins.

Identification of Critical Genes for Recurrent Aphthous Ulcer by Transcriptome Data Analysis and Mendelian Randomization.

CD71-based immature RBC (iRBC) analysis in peripheral blood has a better correlation with leukocyte PNH clone size and improves the delineation of different PNH clone types.

Costello Syndrome Associated With Somatic Mosaicism of Rare p.Gly13Asp HRAS Variant: Expanding the Phenotypic Spectrum.

A novel prognostic model based on Golgi apparatus-related genes predicts patient survival in glioblastoma.

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Reply to a response by Sherman & Iselius to comments on the segregation of balanced pericentric inversions

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