Literature DB >> 15735970

Cantu syndrome.

Thomas E Herman1, William H McAlister.   

Abstract

Entities:  

Mesh：

Year:  2005        PMID： 15735970     DOI： 10.1007/s00247-004-1386-2

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


× No keyword cloud information.
  4 in total

Review 1.  Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).

Authors:  B Lazalde; R Sánchez-Urbina; I Nuño-Arana; W E Bitar; M de Lourdes Ramírez-Dueñas
Journal:  Am J Med Genet       Date:  2000-10-23

2.  Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome.

Authors:  S P Robertson; E Kirk; F Bernier; J Brereton; A Turner; A Bankier
Journal:  Am J Med Genet       Date:  1999-08-06

3.  A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity.

Authors:  J M Cantú; D García-Cruz; J Sánchez-Corona; A Hernández; Z Nazará
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 4.  Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Authors:  Hartmut Engels; Kristin Bosse; Antje Ehrbrecht; Susanne Zahn; Alexander Hoischen; Peter Propping; Lutz Bindl; Heiko Reutter
Journal:  Am J Med Genet       Date:  2002-08-01
  4 in total
  1 in total

1.  Copy number variations on chromosome 4q26-27 are associated with Cantu syndrome.

Authors:  Mazen Kurban; Chong Ae Kim; Maija Kiuru; Katherine Fantauzzo; Rita Cabral; Ossama Abbas; Brynn Levy; Angela M Christiano
Journal:  Dermatology       Date:  2012-02-03       Impact factor: 5.366
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.