Assignment of the Gene Locus for Severe Congenital Neutropenia to Chromosome 1q22 in the Original Kostmann Family From Northern Sweden

Biochemical and Biophysical Research Communications - United States
doi 10.1016/j.bbrc.2006.12.086
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

Severe Congenital Neutropenia

2020English

Autosomal Recessive Severe Congenital Neutropenia Due to G6PC3 Deficiency

2020English

Assignment of the Structural Gene for the Third Component of Human Complement to Chromosome 19.

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1982English

Hematopoietic Stem Cell Transplantation in Severe Congenital Neutropenia: Experience of the French SCN Register

Bone Marrow Transplantation
TransplantationHematology
2004English

A Novel Locus for Congenital Simple Microphthalmia Family Mapping to 17p12-Q12

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2011English

Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia

Frontiers in Immunology
AllergyImmunology
2019English

Congenital Neutropenia

Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer ResearchOncologyGeneticsHematology
2011English

Assignment of Genes Encoding Metallothioneins I and II to Chinese Hamster Chromosome 3: Evidence for the Role of Chromosome Rearrangement in Gene Amplification.

Molecular and Cellular Biology
Cell BiologyMolecular Biology
1984English

Functional Characteristics of Circulating Granulocytes in Severe Congenital Neutropenia Caused by ELANE Mutations

BMC Pediatrics
Child HealthPediatricsPerinatology
2019English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy