rare genetic condition nf1 leads to multiple diagnoses for family | sanford health news
Published 7 months ago • 1.4K plays • Length 3:49Download video MP4
Download video MP3
Similar videos
-
1:00
nf1 patient finds specialized care for rare genetic condition
-
4:02
what is neurofibromatosis type 1 (nf1)?
-
5:45
neurofibromatosis, causes, signs and symptoms, diagnosis and treatment.
-
2:06
mother spreads awareness about rare genetic disorder neurofibromatosis
-
1:00
what is neurofibromatosis?
-
10:45
ern genturis schwannomatosis guidelines
-
2:28
cf foundation | exploring treatments for nonsense and rare mutations
-
1:16
neurofibromatosis type 1: clinical diagnostic criteria
-
8:21
ern genturis clinical guidelines for nf1 patients
-
3:12
a journey with nf - a rare and lifelong condition (neurofibromatosis)
-
4:19
diagnosis of neurofibromatosis type 1
-
26:26
genetic testing for neurofibromatosis
-
4:23
a challenging case of neurofibromatosis
-
3:51
about the rare disease "schwannomatosis"
-
2:16
managing symptoms of nf1
-
6:03
neurofibromatosis types 1 and 2
-
3:47
nf1 versus nf2
-
4:19
diagnosis of neurofibromatosis type 1
-
1:23
how is neurofibromatosis treated?