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Meckel Gruber and Joubert Syndrome Diagnosed Prenatally: Allelism between the Two Ciliopathies, Complexities of Mutation Types and Digenic Inheritance.
Srivastava, Somya; Manisha, Rani; Dwivedi, Aradhana; Agarwal, Harshita; Saxena, Deepti; Agrawal, Vinita; Mandal, Kausik.
Afiliação
  • Srivastava S; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
  • Manisha R; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
  • Dwivedi A; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
  • Agarwal H; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
  • Saxena D; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
  • Agrawal V; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
  • Mandal K; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Science, Lucknow, India.
Fetal Pediatr Pathol ; 41(6): 1041-1051, 2022 Dec.
Article em En | MEDLINE | ID: mdl-34821546

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Anormalidades do Olho / Transtornos da Motilidade Ciliar / Ciliopatias / Doenças Renais Policísticas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Anormalidades do Olho / Transtornos da Motilidade Ciliar / Ciliopatias / Doenças Renais Policísticas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article