Two male sibs with uterus and Fallopian tubes. A rare, probably inherited disorder

(AC)n dinucleotide repeat polymorphism in 5' beta-globin gene in native and Mestizo Mexican populations.

Human biology·2002

Serum-ionized calcium in mexican protein-energy malnourished children.

Archives of medical research·2001

Mexican geneticists' views of ethical issues in genetics testing and screening. Are eugenic principles involved?

Clinical genetics·2000

Mexican geneticists' opinions on disclosure issues.

Clinical genetics·1998

Attitudes of Mexican geneticists towards prenatal diagnosis and selective abortion.

American journal of medical genetics·1998

[Genetic influence on energy requirements. III. Multifactorial inheritance modified by gender].

Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion·1995

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

Clinical genetics·2026

Childhood-Onset Filamin c Related Cardiomyopathy: Genotype-Phenotype Correlation and Outcome.

Clinical genetics·2026

A Homozygous Variant in DMRTB1 Is Associated With Non-Obstructive Azoospermia in Humans.

Clinical genetics·2026

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.

Clinical genetics·2026

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

Clinical genetics·2026

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

Clinical genetics·2026

Determinants of functional burden pleiotropy and gene dosage responses across human traits.

Nature communications·2026

Discovering common and population-specific QTLs for leaf rust resistance in different Barley populations.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Clinical laboratory·2026

Audiological Features in Pendred Syndrome: A Scoping Review.

The journal of international advanced otology·2026

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Journal of blood medicine·2026

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Journal of molecular neuroscience : MN·2026

Related Experiment Videos

Two male sibs with uterus and Fallopian tubes. A rare, probably inherited disorder

Related Concept Videos

(AC)n dinucleotide repeat polymorphism in 5' beta-globin gene in native and Mestizo Mexican populations.

Serum-ionized calcium in mexican protein-energy malnourished children.

Mexican geneticists' views of ethical issues in genetics testing and screening. Are eugenic principles involved?

Mexican geneticists' opinions on disclosure issues.

Attitudes of Mexican geneticists towards prenatal diagnosis and selective abortion.

[Genetic influence on energy requirements. III. Multifactorial inheritance modified by gender].

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

Childhood-Onset Filamin c Related Cardiomyopathy: Genotype-Phenotype Correlation and Outcome.

A Homozygous Variant in DMRTB1 Is Associated With Non-Obstructive Azoospermia in Humans.

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.

Determinants of functional burden pleiotropy and gene dosage responses across human traits.

Discovering common and population-specific QTLs for leaf rust resistance in different Barley populations.

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Audiological Features in Pendred Syndrome: A Scoping Review.

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Related Experiment Videos

Two male sibs with uterus and Fallopian tubes. A rare, probably inherited disorder

Related Concept Videos

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