P869: Expanding the prenatal and postnatal phenotype of 1q21.1 duplication: A case report
Saved in:
| Main Authors: | Zenobia Gonsalves, Rachel Lee, Kimberly Herrera, Jennifer Choi, Chaitali Korgaonkar-Cherala, Cassandra Heiselman |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2025-01-01
|
| Series: | Genetics in Medicine Open |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2949774425012774 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Prenatal ultrasound phenotype of fetuses with recurrent 1q21.1 deletion and duplication syndrome
by: Fengyang Wang, et al.
Published: (2025-01-01) -
A review on the relationship between the distal 1q21.1 microdeletion and schizophrenia
by: Xinpeng Guo, et al.
Published: (2025-07-01) -
Molecular diagnosis and preimplantation genetic testing for chromosome 1q21.1 recurrent microduplication
by: Cuiting Peng, et al.
Published: (2025-03-01) -
P414: Unique case of mosaic 8q21.1-q24.3 deletion and duplications linked to Langer-Giedion and Cornelia de Lange syndromes presenting with recurrent fractures
by: Samuel David Amio Valientes, et al.
Published: (2025-01-01) -
Identification of a Novel 15q21.1 Microdeletion in a Family with Marfan Syndrome
by: Rencong Yang, et al.
Published: (2022-01-01)