Monosomy 1p36: Report of a cohort of 13 Asian Indian patients.

Gupta, Neerja; Kaur, Ravneet; Phadke, Shubha; Sharma, Pankaj; Nampoothiri, Sheela; Saxena, Deepti; Kabra, Madhulika

Gupta, Neerja; Kaur, Ravneet; Phadke, Shubha; Sharma, Pankaj; Nampoothiri, Sheela; Saxena, Deepti; Kabra, Madhulika.

Afiliação

Gupta N; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Kaur R; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Phadke S; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Sharma P; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
Nampoothiri S; Department of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, Cochin, Kerala, India.
Saxena D; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Kabra M; Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.

Am J Med Genet A ; 188(4): 1317-1322, 2022 04.

Article em En | MEDLINE | ID: mdl-34989134

Assuntos

Deleção Cromossômica; Monossomia; Cromossomos Humanos Par 1/genética; Estudos de Coortes; Humanos; Monossomia/genética; Fenótipo

Palavras-chave

1p36 deletion; 1p36 deletion syndrome; monosomy 1p36

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção Cromossômica / Monossomia Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia

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