High-resolution studies of chromosome 10 in 23 MEN-2 families

Factors associated with Noninvasive ventilation compliance in patients with ALS/MND.

Amyotrophic lateral sclerosis & frontotemporal degeneration·2021

Longitudinal associations between post-traumatic stress disorder and metabolic syndrome severity.

Psychological medicine·2016

Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype.

Leukemia·2010

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients.

Leukemia·2010

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Neurology·2009

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Neurology·2009

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Cancer genetics and cytogenetics·2010

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Cancer genetics and cytogenetics·2010

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Cancer genetics and cytogenetics·2010

Screening for common copy-number variants in cancer genes.

Cancer genetics and cytogenetics·2010

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Cancer genetics and cytogenetics·2010

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Cancer genetics and cytogenetics·2010

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Yeast (Chichester, England)·2026

Co-segregation of WFS1 p.Gly494Ser variant with recurrent vasovagal syncope in a multigenerational family: a candidate susceptibility variant needing independent validation.

Frontiers in pediatrics·2026

Chromosome painting in plants: history and future perspectives.

Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology·2026

A chromosome-scale genome of Capsicum pubescens provides insights into candidate terpene-associated gene clusters and pan variation of terpene synthases.

Planta·2026

Identification of Two Novel Compound Heterozygous ADAMTS17 Variants Associated With Weill-Marchesani Syndrome 4.

Laboratory investigation; a journal of technical methods and pathology·2026

Genomic inbreeding coefficients and inbreeding depression of semen production traits at genome-wide and chromosomal levels in Japanese Holstein bulls.

Journal of dairy science·2026

Related Experiment Videos

High-resolution studies of chromosome 10 in 23 MEN-2 families

Related Concept Videos

Factors associated with Noninvasive ventilation compliance in patients with ALS/MND.

Longitudinal associations between post-traumatic stress disorder and metabolic syndrome severity.

Monosomal karyotype in myelodysplastic syndromes, with or without monosomy 7 or 5, is prognostically worse than an otherwise complex karyotype.

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients.

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Screening for common copy-number variants in cancer genes.

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Co-segregation of WFS1 p.Gly494Ser variant with recurrent vasovagal syncope in a multigenerational family: a candidate susceptibility variant needing independent validation.

Chromosome painting in plants: history and future perspectives.

A chromosome-scale genome of Capsicum pubescens provides insights into candidate terpene-associated gene clusters and pan variation of terpene synthases.

Identification of Two Novel Compound Heterozygous ADAMTS17 Variants Associated With Weill-Marchesani Syndrome 4.

Genomic inbreeding coefficients and inbreeding depression of semen production traits at genome-wide and chromosomal levels in Japanese Holstein bulls.

Related Experiment Videos

High-resolution studies of chromosome 10 in 23 MEN-2 families

Related Concept Videos

Related Articles