11p15.4 Microdeletion Associates with Hemihypertrophy
Joint Authors
Puvabanditsin, Surasak
Jacob, Marianne
Jalil, Maaz
Sadiq, Mehrin
Mehta, Rajeev
Cabrera, Kenya
Choudry, Omer
Source
Issue
Vol. 2018, Issue 2018 (31 Dec. 2018), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2018-10-30
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
We report a preterm female infant with intrauterine growth retardation, dysmorphic facies, missing rib, small hands and feet, and hemihypertrophy.
The results of whole genome SNP microarray analysis showed approximately 77 Kb interstitial deletion of the short arm of chromosome 11 (11p15.4).
We report novel clinical findings of this rare genetic condition.
American Psychological Association (APA)
Puvabanditsin, Surasak& Sadiq, Mehrin& Jacob, Marianne& Jalil, Maaz& Cabrera, Kenya& Choudry, Omer…[et al.]. 2018. 11p15.4 Microdeletion Associates with Hemihypertrophy. Case Reports in Genetics،Vol. 2018, no. 2018, pp.1-5.
https://search.emarefa.net/detail/BIM-1143307
Modern Language Association (MLA)
Puvabanditsin, Surasak…[et al.]. 11p15.4 Microdeletion Associates with Hemihypertrophy. Case Reports in Genetics No. 2018 (2018), pp.1-5.
https://search.emarefa.net/detail/BIM-1143307
American Medical Association (AMA)
Puvabanditsin, Surasak& Sadiq, Mehrin& Jacob, Marianne& Jalil, Maaz& Cabrera, Kenya& Choudry, Omer…[et al.]. 11p15.4 Microdeletion Associates with Hemihypertrophy. Case Reports in Genetics. 2018. Vol. 2018, no. 2018, pp.1-5.
https://search.emarefa.net/detail/BIM-1143307
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1143307
