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Items: 12

1.

Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.

Holberg CJ, Erickson RP, Bernas MJ, Witte MH, Fultz KE, Andrade M, Witte CL.

Am J Med Genet. 2001 Feb 1;98(4):303-12.

PMID:
11170072
2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
3.

Pericentric inversions of chromosome 4: report of a new family and review of the literature.

Villa A, Urioste M, Carrascosa MC, Vázquez S, Martínez A, Martínez-Frías ML.

Clin Genet. 1995 Nov;48(5):255-60. Review.

PMID:
8825604
4.

[Genetic aspects of asthma].

Rojas-Martínez A, Santillán AA, Delgado-Enciso I, Barrera-Saldaña HA.

Rev Invest Clin. 2000 Jul-Aug;52(4):441-50. Review. Spanish.

PMID:
11061107
5.

Milroy's primary congenital lymphedema in a male infant and review of the literature.

Kitsiou-Tzeli S, Vrettou C, Leze E, Makrythanasis P, Kanavakis E, Willems P.

In Vivo. 2010 May-Jun;24(3):309-14. Review.

PMID:
20555004
6.

Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications.

Andersson HC, Parry DM, Mulvihill JJ.

Am J Med Genet. 1995 Mar 13;56(1):72-5. Review.

PMID:
7747790
7.

FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update.

Gordon K, Spiden SL, Connell FC, Brice G, Cottrell S, Short J, Taylor R, Jeffery S, Mortimer PS, Mansour S, Ostergaard P.

Hum Mutat. 2013 Jan;34(1):23-31. doi: 10.1002/humu.22223. Epub 2012 Oct 16. Review.

PMID:
23074044
8.

Report of the committee on the genetic constitution of chromosomes 18 and 19.

Le Beau MM, Ryan D Jr, Pericak-Vance MA.

Cytogenet Cell Genet. 1989;51(1-4):338-57. Review. No abstract available.

PMID:
2676376
9.

Report of the committee on the genetic constitution of chromosome 4.

Cox DR, Murray JC, Buetow KH.

Cytogenet Cell Genet. 1989;51(1-4):121-36. Review. No abstract available.

PMID:
2676366
10.

Report of the committee on the genetic constitution of chromosome 11.

Junien C, McBride OW.

Cytogenet Cell Genet. 1989;51(1-4):226-58. Review. No abstract available.

PMID:
2676371
11.

Milroy disease and the VEGFR-3 mutation phenotype.

Brice G, Child AH, Evans A, Bell R, Mansour S, Burnand K, Sarfarazi M, Jeffery S, Mortimer P.

J Med Genet. 2005 Feb;42(2):98-102. Review.

12.

[The trophedema (Nonne-Milroy-Meige). Carcinogenesis as a rare complication].

Köstler E.

Dermatol Monatsschr. 1976 Jun;162(6):465-77. Review. German.

PMID:
786757

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