Monosomy 1p36: Report of a cohort of 13 Asian Indian patients-Reference-Cited by-同舟云学术

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

Published:2022-01-06 Issue:4 Volume:188 Page:1317-1322
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Gupta Neerja¹^ORCID,Kaur Ravneet¹^ORCID,Phadke Shubha²^ORCID,Sharma Pankaj¹^ORCID,Nampoothiri Sheela³^ORCID,Saxena Deepti²^ORCID,Kabra Madhulika¹

Affiliation:

1. Division of Genetics, Department of Pediatrics All India Institute of Medical Sciences New Delhi India

2. Department of Medical Genetics Sanjay Gandhi Post Graduate Institute of Medical Sciences Lucknow Uttar Pradesh India

3. Department of Pediatric Genetics Amrita Institute of Medical Sciences & Research Centre Cochin Kerala India

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62630

Reference20 articles.

1. Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation

2. Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathy

3. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia

4. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems

5. Physical Map of 1p36, Placement of Breakpoints in Monosomy 1p36, and Clinical Characterization of the Syndrome

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