Legius Syndrome - an overview
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Descrição
Café au Lait Macules and Associated Genetic Syndromes - ScienceDirect
Noonan syndrome: MedlinePlus Genetics
Café-Au-Lait Macules and Macrocephaly in a 19-Month-Old: Diagnostic Considerations Beyond Neurofibromatosis – Consult QD
Part 1: Café-au-lait macule – Presentation and genesis
Noonan syndrome: improving recognition and diagnosis
PDF] Legius syndrome, an Update. Molecular pathology of mutations in SPRED1.
IJMS, Free Full-Text
Café-au-lait macule differential by craniofacial examination. Many of
Novel association of neurofibromatosis type 1‐causing mutations in families with neurofibromatosis‐noonan syndrome - Ekvall - 2014 - American Journal of Medical Genetics Part A - Wiley Online Library
Photographs of selected individuals with syndromes of the Ras pathway.
Children, Free Full-Text
Pediatric Dermatology Consult - December 2016
Cureus, Neurofibromatosis-Noonan Syndrome With Primary Amenorrhoea: A Case Report
Café-Au-Lait Macules and Macrocephaly in a 19-Month-Old: Diagnostic Considerations Beyond Neurofibromatosis – Consult QD
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