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Results: 4

1.

Terminal deletion 2q37.3 in a patient with Klippel-Trenaunay-Weber syndrome.

Puiu I, Stoica A, Sosoi S, Puiu A, Ioana M, Burada F.

Fetal Pediatr Pathol. 2013 Oct;32(5):351-6. doi: 10.3109/15513815.2013.768739. Epub 2013 Feb 25.

PMID:
23438794
[PubMed - indexed for MEDLINE]
2.

The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients.

Leroy C, Landais E, Briault S, David A, Tassy O, Gruchy N, Delobel B, Grégoire MJ, Leheup B, Taine L, Lacombe D, Delrue MA, Toutain A, Paubel A, Mugneret F, Thauvin-Robinet C, Arpin S, Le Caignec C, Jonveaux P, Beri M, Leporrier N, Motte J, Fiquet C, Brichet O, Mozelle-Nivoix M, Sabouraud P, Golovkine N, Bednarek N, Gaillard D, Doco-Fenzy M.

Eur J Hum Genet. 2013 Jun;21(6):602-12. doi: 10.1038/ejhg.2012.230. Epub 2012 Oct 17.

PMID:
23073310
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Medullary thyroid carcinoma and 2q37 deletion in a patient with nevoid basal cell carcinoma syndrome: clinical description and genetic analysis.

Coca-Pelaz A, Llorente-Pendás JL, García-Martínez J, Vivanco-Allende B, Balbín M, Suárez C, Hermsen M.

Head Neck. 2013 May;35(5):E147-52. doi: 10.1002/hed.22000. Epub 2012 Feb 9.

PMID:
22319002
[PubMed - indexed for MEDLINE]
4.

Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.

Devillard F, Guinchat V, Moreno-De-Luca D, Tabet AC, Gruchy N, Guillem P, Nguyen Morel MA, Leporrier N, Leboyer M, Jouk PS, Lespinasse J, Betancur C.

Am J Med Genet A. 2010 Sep;152A(9):2346-54. doi: 10.1002/ajmg.a.33601.

PMID:
20684015
[PubMed - indexed for MEDLINE]

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