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Academic Journal

Neuropathology of trisomy 21 mosaicism in a case with early‐onset dementia

Authors : Ngo, Phong T; Pascual, Jesse R; Wright, Sierra

Subjects: Biomedical and Clinical Sciences; Biological Psychology; Clinical Sciences

Source: Alzheimer's & Dementia. 21(1)

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Academic Journal

Chromosome 9p trisomy increases stem cells clonogenic potential and fosters T-cell exhaustion in JAK2-mutant myeloproliferative neoplasms

Authors : Carretta, Chiara; Parenti, Sandra; Bertesi, Matteo

Subjects: Male; Adult; Myeloproliferative Disorders

Source: Leukemia

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Academic Journal

Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome

Authors : Chih-Ping Chen; Fang-Tzu Wu; Yen-Ting Pan

Subjects: Adult; Male; Comparative Genomic Hybridization

Source: Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 3, Pp 394-397 (2024)

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Academic Journal

Clinical course and genetic analysis of a case of the amniocentesis showing chromosome 6 trisomy mosaicism

Authors : Naoya Kitamura; Yuki Ito; Tomoko Kawai

Subjects: Male; Adult; 0301 basic medicine

Source: Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 3, Pp 418-421 (2024)

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Academic Journal

Rapid detection of paternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction analysis in a fetus associated with increased nuchal translucency thickness and in a pregnancy without an advanced maternal age

Authors : Chih-Ping Chen

Subjects: Adult; Male; Pregnancy

Source: Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 4, Pp 565-567 (2024)

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Academic Journal

Trends in the survival of patients with trisomy 13 from 1995 to 2021: A population study in Japan

Authors : Narumi Kato; Naho Morisaki; Akinori Moriichi

Subjects: Male; Adult; 0301 basic medicine

Source: American Journal of Medical Genetics Part A. 194

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Academic Journal

Prevalence and clinical characterization of oral clefts in patients with chromosome trisomy 18

Authors : Nadini Cristina Marins Martinez; Sheila Tamanini de Almeida; Rafael Fabiano Machado Rosa

Subjects: Male; Adolescent; Cleft Lip

Source: Rev Paul PediatrRevista Paulista de Pediatria, Vol 42 (2024)

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Academic Journal

A case of Behçet’s-like disease associated with trisomy 8–positive myelodysplastic syndrome carrying MEFV E148Q variant presented with periodic fever

Authors : Yukiko Ishikawa; Ryo Sasaki; Akira Ishiwata

Subjects: Male; Aged, 80 and over; Fever

Source: Modern Rheumatology Case Reports. 7:470-474

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Academic Journal

Treatment of Iliac Arteriovenous Malformation Associated with Trisomy 21: A Case Report

Authors : Jinming Yang; Weichao Zhao; Liping Liang

Subjects: Adult; Male; Iliac arteriovenous malformation

Source: J Cardiothorac SurgJournal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-6 (2024)

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Academic Journal

Congenital Anomalies of the Gastrointestinal Tract in Conjunction of Congenital Heart Diseases in Infants With Trisomy 21

Authors : Allison M. Peluso; Mohsen A. A. Farghaly; Hany Aly

Subjects: Heart Defects, Congenital; Male; Gastrointestinal Tract

Source: Birth Defects Research. 116

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نتائج البحث

فلترة النتائج

Neuropathology of trisomy 21 mosaicism in a case with early‐onset dementia

Chromosome 9p trisomy increases stem cells clonogenic potential and fosters T-cell exhaustion in JAK2-mutant myeloproliferative neoplasms

Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome

Clinical course and genetic analysis of a case of the amniocentesis showing chromosome 6 trisomy mosaicism

Rapid detection of paternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction analysis in a fetus associated with increased nuchal translucency thickness and in a pregnancy without an advanced maternal age

Trends in the survival of patients with trisomy 13 from 1995 to 2021: A population study in Japan

Prevalence and clinical characterization of oral clefts in patients with chromosome trisomy 18

A case of Behçet’s-like disease associated with trisomy 8–positive myelodysplastic syndrome carrying MEFV E148Q variant presented with periodic fever

Treatment of Iliac Arteriovenous Malformation Associated with Trisomy 21: A Case Report

Congenital Anomalies of the Gastrointestinal Tract in Conjunction of Congenital Heart Diseases in Infants With Trisomy 21

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