Your browser doesn't support javascript.
loading
Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature.
Upadhyai, Priyanka; Amiri, Eram Fatima; Guleria, Vishal Singh; Bielas, Stephanie L; Girisha, Katta Mohan; Shukla, Anju.
Afiliação
  • Upadhyai P; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
  • Amiri EF; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
  • Guleria VS; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
  • Bielas SL; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.
  • Girisha KM; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
  • Shukla A; Department of Medical Genetics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Clin Dysmorphol ; 29(3): 127-131, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32459673
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Megalencefalia Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Clin Dysmorphol Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Megalencefalia Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Clin Dysmorphol Ano de publicação: 2020 Tipo de documento: Article