Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18

Trisomy 21 mosaicism: we may all have a touch of Down syndrome.

Cytogenetic and genome research·2013

Loss of heterozygosity at chromosome 6q correlates with tumor progression and patient survival.

International journal of oncology·2011

Loss of heterozygosity at chromosome 1p in human breast cancer.

International journal of oncology·2011

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients.

Clinical genetics·2008

An Internet-based weight loss programme -- a feasibility study with preliminary results from 4209 completers.

Scandinavian journal of public health·2008

Extensive intestinal metaplasia in gastric carcinoma and in other lesions requiring surgery: a study of 3,421 gastrectomy specimens from dwellers of the Atlantic and Pacific basins.

Journal of clinical pathology·2005

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Annales de genetique·2004

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Annales de genetique·2004

Large duplication 4q25-q34 with mild clinical effect.

Annales de genetique·2004

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Annales de genetique·2004

Partial trisomy 8q and partial monosomy 18p: a case report.

Annales de genetique·2004

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Annales de genetique·2004

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Molecular biology and evolution·2026

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Brain communications·2026

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Brain, behavior, and immunity·2026

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

Legal medicine (Tokyo, Japan)·2026

LINE-1 repeats are a defining feature of the Xce.

Proceedings of the National Academy of Sciences of the United States of America·2026

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

JCI insight·2026

Related Experiment Videos

Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18

Related Concept Videos

Trisomy 21 mosaicism: we may all have a touch of Down syndrome.

Loss of heterozygosity at chromosome 6q correlates with tumor progression and patient survival.

Loss of heterozygosity at chromosome 1p in human breast cancer.

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients.

An Internet-based weight loss programme -- a feasibility study with preliminary results from 4209 completers.

Extensive intestinal metaplasia in gastric carcinoma and in other lesions requiring surgery: a study of 3,421 gastrectomy specimens from dwellers of the Atlantic and Pacific basins.

Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending.

Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia.

Large duplication 4q25-q34 with mild clinical effect.

A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES).

Partial trisomy 8q and partial monosomy 18p: a case report.

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

LINE-1 repeats are a defining feature of the Xce.

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

Related Experiment Videos

Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18

Related Concept Videos

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