Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by L. Micale
Report of the First Clinical Case of a Moroccan Kabuki Patient With a Novel MLL2 Mutation
Molecular Syndromology
Genetics
Related publications
A Novel Frameshift Mutation in the XPC Gene in a Moroccan Patient: A Case Report
Journal of Medical Case Reports
Medicine
Clinical and Molecular Report of Novel GALC Mutations in Moroccan Patient With Krabbe Disease: Case Report
BMC Pediatrics
Child Health
Pediatrics
Perinatology
A Novel TRPS1 Mutation in a Moroccan Family With Tricho-Rhino-Phalangeal Syndrome Type III: Case Report
BMC Medical Genetics
Genetics
Down Syndrome Associated With Clinical Manifestations of Kabuki Syndrome: Report of a Case
Jornal de Pediatria
Child Health
Pediatrics
Perinatology
A Novel BRCA1 Mutation in a Patient With Breast and Ovarian Cancer: A Case Report
Oncology Letters
Cancer Research
Oncology
Identification of a Novel Splicing Mutation in the SLC25A13 Gene From a Patient With NICCD: A Case Report
BMC Pediatrics
Child Health
Pediatrics
Perinatology
A Case Report of a Symptomatic Osteopoikilosis Patient Caused by Novel Mutation in LEMD3
Endocrine Abstracts
Eleven Percent Intact PGM3 in a Severely Immunodeficient Patient With a Novel Splice-Site Mutation, a Case Report
BMC Pediatrics
Child Health
Pediatrics
Perinatology
Primary Amenorrhea in Kabuki Syndrome: A Case Report
International Journal of Anatomy and Research