The prenatal diagnosis of an 8p23.1 deletion is reported. The diagnosis was ascertained at 22 weeks of gestation because of the discovery of a diaphragmatic hernia at ultrasound. Following cytogenetic studies and counselling, the pregnancy was terminated. An autopsy confirmed the presence of a diaph
β¦ LIBER β¦
Prenatal diagnosis of 5p deletion syndrome in a female fetus leading to identification of the same diagnosis in her mother
β Scribed by Nguyen, Joanne Macayran; Gamble, Candace; Smith, Janice L.; Raia, Marianna; Johnson, Anthony; Czerwinski, Jennifer
- Book ID
- 126833626
- Publisher
- John Wiley and Sons
- Year
- 2014
- Tongue
- English
- Weight
- 488 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0197-3851
- DOI
- 10.1002/pd.4436
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