Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children
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| Veröffentlicht in: | American journal of medical genetics. Part A 2021-12, Vol.185 (12), p.3895-3896 |
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| container_end_page | 3896 |
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| container_issue | 12 |
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| container_title | American journal of medical genetics. Part A |
| container_volume | 185 |
| creator | Calligaris, Lorenzo Cortellazzo Wiel, Luisa Sartor, Emma Berti, Irene Bruno, Irene Barbi, Egidio Magnolato, Andrea |
| description | |
| doi_str_mv | 10.1002/ajmg.a.62420 |
| format | Article |
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| identifier | ISSN: 1552-4825 |
| ispartof | American journal of medical genetics. Part A, 2021-12, Vol.185 (12), p.3895-3896 |
| issn | 1552-4825 1552-4833 |
| language | eng |
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| source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
| subjects | Adolescent Child Child, Preschool Female Genetic disorders Genetic Predisposition to Disease Humans Infant Male Neurofibromatosis Neurofibromatosis 1 - complications Neurofibromatosis 1 - diagnosis Neurofibromatosis 1 - genetics Neurofibromatosis 1 - pathology Neurological disorders Recklinghausen's disease Risk Factors Tumors Xanthogranuloma, Juvenile - complications Xanthogranuloma, Juvenile - diagnosis Xanthogranuloma, Juvenile - genetics Xanthogranuloma, Juvenile - pathology |
| title | Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children |
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