Doorgaan naar hoofdnavigatie
Doorgaan naar zoeken
Ga verder naar hoofdinhoud
Sorteer per
Keyphrases
Kallmann Syndrome
100%
CHD7 mutation
100%
CHARGE Syndrome
100%
Clinical Overlap
100%
Hypogonadotropic Hypogonadism
66%
CHD7
66%
Anosmia
33%
Clinical Features
16%
Fibroblast Growth Factor Receptor 1 (FGFR1)
16%
De-novo mutations
16%
Aplasia
16%
Hypoplasia
16%
KAL1
16%
CHD7 Gene
16%
PROKR2
16%
Semicircular Canal
16%
Deafness
16%
Body Dysmorphic Disorder
16%
Hyposmia
16%
PROK2
16%
Medicine and Dentistry
Kallmann Syndrome
100%
Syndrome CHARGE
100%
CHD7
100%
Hypogonadotropic Hypogonadism
57%
Anosmia
28%
Clinical Feature
14%
Hearing Impairment
14%
Hypoplasia
14%
Aplasia
14%
Semicircular Canal
14%
Hyposmia
14%
Fibroblast Growth Factor Receptor 1
14%
Nursing and Health Professions
Syndrome CHARGE
100%
Kallmann Syndrome
100%
Hypogonadotropic Hypogonadism
66%
Anosmia
33%
Hearing Impairment
16%
Clinical Feature
16%
Hypoplasia
16%
Hyposmia
16%
Aplasia
16%
Fibroblast Growth Factor Receptor 1
16%
Neuroscience
CHD7
100%
Hypogonadotropic Hypogonadism
57%
Anosmia
28%
Hypoplasia
14%
Semicircular Canal
14%
Hyposmia
14%
Fibroblast Growth Factor Receptor 1
14%
Biochemistry, Genetics and Molecular Biology
CHD7
100%
Fibroblast Growth Factor Receptor 1
14%