Skip to content
Hjälp oss att hjälpa fler människor

Jacobsens syndrom > Publikationer

Deletion of ETS-1, a gene in the Jacobsen syndrome critical region, causes ventricular septal defects and abnormal ventricular morphology in mice.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807373/
av Teresa
Sjukvårdspersonal

Jacobsen syndrome

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670819/
av Teresa
Sjukvårdspersonal

Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050515/
av Teresa
Sjukvårdspersonal

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

https://www.ncbi.nlm.nih.gov/m/pubmed/7603564/?i=33&from=mattina%20t
av Teresa
Sjukvårdspersonal

Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.

https://www.ncbi.nlm.nih.gov/m/pubmed/8882392/?i=31&from=mattina%20t
av Teresa
Sjukvårdspersonal

Clinical and molecular characterization of patients with distal 11q deletions.

https://www.ncbi.nlm.nih.gov/m/pubmed/7887422/?i=34&from=mattina%20t
av Teresa
Sjukvårdspersonal

The 11q terminal deletion disorder: a prospective study of 110 cases.

https://www.ncbi.nlm.nih.gov/m/pubmed/15266616/?i=23&from=mattina%20t
av Teresa
Sjukvårdspersonal

Dysmegakaryopoietic thrombocytopenia in patients with distal chromosome 11q deletion.

https://www.ncbi.nlm.nih.gov/m/pubmed/8639871/?i=30&from=mattina%20t
av Teresa
Sjukvårdspersonal