A rare mutation in a patient with Noonan syndrome with multiple lentigines
Saved in:
Main Authors: | Manuel E. Blanco-Cintrón, MD (Author), Fabiola Pabón-González, BS (Author), Xavier Sánchez-Flores, MD (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2023-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Multiple lentigines in RASA1-associated capillary malformation-arteriovenous malformation syndrome
by: Rujira Rujiwetpongstorn, MD, et al.
Published: (2021) -
Cutaneous T-cell lymphoma in SHOC2 mutation-associated Noonan-like syndrome with loose anagen hair
by: Alexandria Avery, DO, et al.
Published: (2022) -
Noonan Syndrome with cleft palate: A rare case report
by: Munish Kumar, et al.
Published: (2016) -
Noonan Syndrome
by: Dina D., et al.
Published: (2018) -
An atypical case of Noonan syndrome with mutation diagnosed by targeted exome sequencing
by: Jinsup Kim, et al.
Published: (2017)