Three non-mongoloid patients of similar phenotype with an extra G-like chromosome

Re-evaluation of the dysequilibrium syndrome.

Acta neurologica Scandinavica·2010

Chromosomal abnormalities and DNA image cytometry of haematological neoplasms in fine needle aspirates of lymph nodes.

Cytopathology : official journal of the British Society for Clinical Cytology·2003

Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study.

Acta paediatrica (Oslo, Norway : 1992)·2002

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Acta dermato-venereologica·1999

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Annals of neurology·1999

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.

Clinical genetics·1998

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy.

Clinical genetics·2026

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

Maternal arsenic exposure induces autism-like behaviors via astrocyte-mediated neuronal apoptosis: Protective effects of Taurine.

Ecotoxicology and environmental safety·2026

The attitude of (would-be) recipients of donor sperm and interested persons regarding a worldwide family limit per donor.

Journal of assisted reproduction and genetics·2026

[Giant Aortic Aneurysm Caused by a Late Complication of Untreated Syphilis:Report of a Case].

Kyobu geka. The Japanese journal of thoracic surgery·2026

Alcohol-induced mortality among Asian Americans, 2018-2022.

Journal of ethnicity in substance abuse·2026

Cancer incidence trends among Asian American, Native Hawaiian, and Pacific Islander populations in the United States, 2000-2022.

Journal of the National Cancer Institute·2026

Neighborhood physical disorder and social participation among older Americans: mediations of social cohesion and depressive symptoms.

Aging & mental health·2026

Related Experiment Videos

Three non-mongoloid patients of similar phenotype with an extra G-like chromosome

Related Concept Videos

Re-evaluation of the dysequilibrium syndrome.

Chromosomal abnormalities and DNA image cytometry of haematological neoplasms in fine needle aspirates of lymph nodes.

Prevalence and associated impairments of mild mental retardation in six- to ten-year old children in Pakistan: a prospective study.

Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding.

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy.

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.

Maternal arsenic exposure induces autism-like behaviors via astrocyte-mediated neuronal apoptosis: Protective effects of Taurine.

The attitude of (would-be) recipients of donor sperm and interested persons regarding a worldwide family limit per donor.

[Giant Aortic Aneurysm Caused by a Late Complication of Untreated Syphilis:Report of a Case].

Alcohol-induced mortality among Asian Americans, 2018-2022.

Cancer incidence trends among Asian American, Native Hawaiian, and Pacific Islander populations in the United States, 2000-2022.

Neighborhood physical disorder and social participation among older Americans: mediations of social cohesion and depressive symptoms.

Related Experiment Videos

Three non-mongoloid patients of similar phenotype with an extra G-like chromosome

Related Concept Videos

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