PubMed

Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation.

Whelan AJ, Watson MS, Porter FD, Steiner RD.

Am J Med Genet. 1995 Dec 4;59(4):492-4.PMID: 8585570 [PubMed - indexed for MEDLINE]Related articles

A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritance.

Ceballos-Quintal JM, Pinto-Escalante D, Castillo-Zapata I.

Am J Med Genet. 1996 Jun 14;63(3):426-7.PMID: 8737646 [PubMed - indexed for MEDLINE]Related articles

[A case of Klippel-Trenaunay-Weber syndrome--special reference to myelopathy]

Moritoyo T, Hashimoto K, Furuzono H, Nagamatsu K.

Rinsho Shinkeigaku. 1993 Jul;33(7):746-53. Japanese. PMID: 8252827 [PubMed - indexed for MEDLINE]Related articles

Extradural thoracic arteriovenous malformation in a patient with Klippel-Trenaunay-Weber syndrome: case report.

Alexander MJ, Grossi PM, Spetzler RF, McDougall CG.

Neurosurgery. 2002 Nov;51(5):1275-8; discussion 1278-9.PMID: 12383373 [PubMed - indexed for MEDLINE]Related articles

[An adult case of congenital Horner's syndrome with heterochromia iridis--with special reference to alteration of Horner's sign associated with development]

Uyama E, Maeda J, Adachi K, Yu TC, Araki S.

Rinsho Shinkeigaku. 1989 Oct;29(10):1278-82. Review. Japanese. PMID: 2691167 [PubMed - indexed for MEDLINE]Related articles

Prenatal sonographic diagnosis of Klippel-Trenaunay-Weber syndrome associated with umbilical cord hemangioma.

Sahinoglu Z, Uludogan M, Delikara NM.

Am J Perinatol. 2003 Jan;20(1):1-6.PMID: 12638074 [PubMed - indexed for MEDLINE]Related articles

Peripapillary staphyloma associated with orofacial capillary hemangioma.

Kiratli H, Bozkurt B, Mocan C.

Ophthalmic Genet. 2001 Dec;22(4):249-53.PMID: 11803491 [PubMed - indexed for MEDLINE]Related articles

Coarctation of the left pulmonary artery: effects on the pulmonary vasculature of infants.

Zevallos-Giampietri EA, Thelmo WL, Anderson VM.

Pediatr Cardiol. 1997 Sep-Oct;18(5):376-80.PMID: 9270109 [PubMed - indexed for MEDLINE]Related articles

Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)].

Freeman SB, Muralidharan K, Pettay D, Blackston RD, May KM.

Am J Med Genet. 1996 Feb 2;61(4):340-4.PMID: 8834045 [PubMed - indexed for MEDLINE]Related articles

[Thoracic outlet syndrome due to first rib anomaly: a case report]

Hashimoto H, Nikaido Y, Kurokawa S, Miyamoto K, Sakaki T.

No Shinkei Geka. 1994 Nov;22(11):1063-6. Japanese. PMID: 7816178 [PubMed - indexed for MEDLINE]Related articles

Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation.

Fried K, Tieder M, Beer S, Rosenblatt M, Krespin HI.

J Med Genet. 1977 Feb;14(1):68-72.PMID: 839506 [PubMed - indexed for MEDLINE]Related articlesFree article

[A rare form of aortic arch anomaly: left aortic and right descending aortic arch]

Planché C, Roussin R, Paul JF, Belli E, Serraf A.

Arch Mal Coeur Vaiss. 2004 May;97(5):549-53. French. PMID: 15214563 [PubMed - indexed for MEDLINE]Related articles

Congenital hemihypertrophy associated with posterior interosseous nerve entrapment.

Dumitru D, Walsh N, Visser B.

Arch Phys Med Rehabil. 1988 Sep;69(9):696-8.PMID: 3421825 [PubMed - indexed for MEDLINE]Related articles

Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t(12;16)(q13;p11) in myxoid liposarcomas.

Turc-Carel C, Limon J, Dal Cin P, Rao U, Karakousis C, Sandberg AA.

Cancer Genet Cytogenet. 1986 Dec;23(4):291-9.PMID: 3779625 [PubMed - indexed for MEDLINE]Related articles

Interstitial deletion of the short arm of chromosome 12 during clonal evolution in myelodysplastic syndrome with t(5;12)(q13;p13) involving the ETV6 gene.

Yamamoto K, Nagata K, Yagasaki F, Tsurukubo Y, Tamura A, Taniwaki M, Hamaguchi H.

Cancer Genet Cytogenet. 2000 Jun;119(2):113-7. Review.PMID: 10867145 [PubMed - indexed for MEDLINE]Related articles

Grip reconstruction by double-toe transplantation in cases of a fingerless hand and a handless arm.

Holle J, Freilinger G, Mandl H, Frey M.

Plast Reconstr Surg. 1982 Jun;69(6):962-8.PMID: 7079404 [PubMed - indexed for MEDLINE]Related articles

Translocation t(12;16)(q13;p11) in myxoid liposarcoma of a child and implication of the human int-1 gene in tumorigenesis.

Fujii Y, Matui Y, Nakagawa Y, Hongo T, Igarashi Y, Yamada M, Nakagome Y, Tobayama S.

Jpn J Cancer Res. 1989 Oct;80(10):958-62.PMID: 2515180 [PubMed - indexed for MEDLINE]Related articles

Spindle cell vulvar hemangiomatosis associated with enchondromatosis: a rare variant of Maffucci's syndrome.

Fernández-Aguilar S, Fayt I, Noël JC.

Int J Gynecol Pathol. 2004 Jan;23(1):68-70.PMID: 14668554 [PubMed - indexed for MEDLINE]Related articles

Anomalous origin of either the right or left main coronary artery from the aorta with subsequent coursing between aorta and pulmonary trunk: analysis of 32 necropsy cases.

Kragel AH, Roberts WC.

Am J Cardiol. 1988 Oct 1;62(10 Pt 1):771-7.PMID: 3421178 [PubMed - indexed for MEDLINE]Related articles

Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).

Fryns JP, Kleczkowska A, Smeets E, Thiry P, Geutjens J, Van den Berghe H.

Am J Med Genet. 1990 Dec;37(4):546-7.PMID: 2260606 [PubMed - indexed for MEDLINE]Related articles