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First case report of Penttinen syndrome from India.
Aggarwal, Bhawana; Correa, Alec R E; Gupta, Neerja; Jana, Manisha; Kabra, Madhulika.
Afiliação
  • Aggarwal B; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Correa ARE; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Gupta N; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
  • Jana M; Department of Radio-Diagnosis, All India Institute of Medical Sciences, New Delhi, India.
  • Kabra M; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Am J Med Genet A ; 188(2): 683-687, 2022 02.
Article em En | MEDLINE | ID: mdl-34799960
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progéria / Deformidades Congênitas dos Membros / Senilidade Prematura / Acro-Osteólise Limite: Aged / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Progéria / Deformidades Congênitas dos Membros / Senilidade Prematura / Acro-Osteólise Limite: Aged / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article