Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch-Reference-Cited by-同舟云学术

Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch

Author:

Ibrahim Masitah¹,Hunter Matthew²³,Gugasyan Lucy⁴,Chan Yuen⁵,Malhotra Atul¹³⁶,Sehgal Arvind¹³⁶,Tan Kenneth¹³⁶

Affiliation:

1. Monash Newborn; Monash Medical Centre; Melbourne Victoria Australia

2. Monash Genetics; Monash Medical Centre; Melbourne Victoria Australia

3. Department of Paediatrics; Monash University; Melbourne Victoria Australia

4. Cytogenetics Laboratory, Pathology; Monash Medical Centre; Melbourne Victoria Australia

5. Anatomical Pathology Services; Monash Medical Centre; Melbourne Victoria Australia

6. The Ritchie Centre; Hudson Institute of Medical Research; Clayton Victoria Australia

Funder

Wellcome Trust

Publisher

Wiley

Subject

General Medicine

Reference27 articles.

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