[From Noonan syndrome to juvenile myelomonocytic leukemia]

Arch Pediatr. 2008 Jun;15(5):812-3. doi: 10.1016/S0929-693X(08)71922-5.

[Article in French]

Authors

H Cavé¹, J Lachenaud, B Perez, A Verloes, C Chomienne, B Cassinat

Affiliation

¹ AP-HP, Département de Génétique, Hôpital Robert Debré, 48 boulevard Sérurier, 75019 Paris et INSERM U718. [email protected] <[email protected]>

PMID: 18582761
DOI: 10.1016/S0929-693X(08)71922-5

No abstract available

MeSH terms

Child
Humans
Leukemia, Myelomonocytic, Acute / epidemiology*
Leukemia, Myelomonocytic, Acute / therapy
Noonan Syndrome / complications*
Noonan Syndrome / genetics
Noonan Syndrome / pathology
Prognosis
Protein Tyrosine Phosphatase, Non-Receptor Type 1 / genetics

Substances

PTPN1 protein, human
Protein Tyrosine Phosphatase, Non-Receptor Type 1