These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 15735970)

  • 1. Cantu syndrome.
    Herman TE; McAlister WH
    Pediatr Radiol; 2005 May; 35(5):550-1. PubMed ID: 15735970
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital hypertrichosis, cardiomegaly, and osteochondrodysplasia (Cantú syndrome): a new case with unusual radiological findings.
    Concolino D; Formicola S; Camera G; Strisciuglio P
    Am J Med Genet; 2000 May; 92(3):191-4. PubMed ID: 10817653
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital hypertrichosis, cardiomegaly and mild osteochondrodysplasia.
    Nevin NC; Mulholland HC; Thomas PS
    Am J Med Genet; 1996 Dec; 66(1):33-8. PubMed ID: 8957508
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome.
    Robertson SP; Kirk E; Bernier F; Brereton J; Turner A; Bankier A
    Am J Med Genet; 1999 Aug; 85(4):395-402. PubMed ID: 10398267
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome.
    Garcia-Cruz D; Sánchez-Corona J; Nazará Z; Garcia-Crúz MO; Figuera LE; Castañeda V; Cantú JM
    Am J Med Genet; 1997 Mar; 69(2):138-51. PubMed ID: 9056550
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A familial case of Cantu craniofaciofronto digital syndrome.
    Garcia-Gonzalez CL; Garcia-Cruz D; Garcia-Cruz MO; Castañeda-Cisneros G; Garcia-Ortiz JE; Orozco-Gutiérrez MH; Sanchez-Corona J
    Clin Dysmorphol; 2012 Jul; 21(3):162-166. PubMed ID: 22504422
    [No Abstract]   [Full Text] [Related]  

  • 7. Cantú syndrome with coexisting familial pituitary adenoma.
    Marques P; Spencer R; Morrison PJ; Carr IM; Dang MN; Bonthron DT; Hunter S; Korbonits M
    Endocrine; 2018 Mar; 59(3):677-684. PubMed ID: 29327300
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Three-dimensional facial morphology in Cantú syndrome.
    Roessler HI; Shields K; Grange DK; Knoers NVAM; van Haaften G; Hammond P; van Haelst MM
    Am J Med Genet A; 2020 May; 182(5):1041-1052. PubMed ID: 32100467
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).
    Lazalde B; Sánchez-Urbina R; Nuño-Arana I; Bitar WE; de Lourdes Ramírez-Dueñas M
    Am J Med Genet; 2000 Oct; 94(5):421-7. PubMed ID: 11050630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pulmonary hypertension secondary to partial pulmonary venous obstruction in a child with Cantu syndrome.
    Kobayashi D; Cook AL; Williams DA
    Pediatr Pulmonol; 2010 Jul; 45(7):727-9. PubMed ID: 20575102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
    Engels H; Bosse K; Ehrbrecht A; Zahn S; Hoischen A; Propping P; Bindl L; Reutter H
    Am J Med Genet; 2002 Aug; 111(2):205-9. PubMed ID: 12210352
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aortic aneurysm and craniosynostosis in a family with Cantu syndrome.
    Hiraki Y; Miyatake S; Hayashidani M; Nishimura Y; Matsuura H; Kamada M; Kawagoe T; Yunoki K; Okamoto N; Yofune H; Nakashima M; Tsurusaki Y; Satisu H; Murakami A; Miyake N; Nishimura G; Matsumoto N
    Am J Med Genet A; 2014 Jan; 164A(1):231-6. PubMed ID: 24352916
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurologic and neuroimaging manifestations of Cantú syndrome: A case series.
    Leon Guerrero CR; Pathak S; Grange DK; Singh GK; Nichols CG; Lee JM; Vo KD
    Neurology; 2016 Jul; 87(3):270-6. PubMed ID: 27316244
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cantú syndrome: report of nine new cases and expansion of the clinical phenotype.
    Scurr I; Wilson L; Lees M; Robertson S; Kirk E; Turner A; Morton J; Kidd A; Shashi V; Stanley C; Berry M; Irvine AD; Goudie D; Turner C; Brewer C; Smithson S
    Am J Med Genet A; 2011 Mar; 155A(3):508-18. PubMed ID: 21344641
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil.
    Ohko K; Nakajima K; Nakajima H; Hiraki Y; Kubota K; Fukao T; Miyatake S; Matsumoto N; Sano S
    J Dermatol; 2020 Mar; 47(3):306-310. PubMed ID: 31907964
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cantu syndrome: A longitudinal review of vascular findings in three individuals.
    Parrott A; Lombardo R; Brown N; Tretter JT; Riley L; Weaver KN
    Am J Med Genet A; 2020 May; 182(5):1243-1248. PubMed ID: 32065455
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations.
    Grange DK; Lorch SM; Cole PL; Singh GK
    Am J Med Genet A; 2006 Aug; 140(15):1673-80. PubMed ID: 16835932
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cantu syndrome and lymphoedema.
    García-Cruz D; Mampel A; Echeverria MI; Vargas AL; Castañeda-Cisneros G; Davalos-Rodriguez N; Patiño-Garcia B; Garcia-Cruz MO; Castañeda V; Cardona EG; Marin-Solis B; Cantu JM; Nuñez-Reveles N; Moran-Moguel C; Thavanati PKR; Ramirez-Garcia S; Sanchez-Corona J
    Clin Dysmorphol; 2011 Jan; 20(1):32-37. PubMed ID: 20890180
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry.
    Grange DK; Roessler HI; McClenaghan C; Duran K; Shields K; Remedi MS; Knoers NVAM; Lee JM; Kirk EP; Scurr I; Smithson SF; Singh GK; van Haelst MM; Nichols CG; van Haaften G
    Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):658-681. PubMed ID: 31828977
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical and Molecular Delineation of a Novel Cys1050Phe Missense Mutation in the ABCC9 Gene in a Korean Patient with Cantú Syndrome.
    Kim H; Kim S; Jeon H; Kim J; Yoo J; Seong M; Park S
    Clin Lab; 2017 May; 63(5):991-995. PubMed ID: 28627835
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.