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Mutations in Fibroblast Growth Factor Receptor 1 Cause Both..:

Pitteloud, Nelly ; Acierno Jr., James S. ; Meysing, Astrid...
Proceedings of the National Academy of Sciences of the United States of America. 103 (2006) 16 - p. 6281-6286 , 2006

Link: https://www.jstor.org/stable/30051458

RT Journal
T1 <Title>Mutations in Fibroblast Growth Factor Receptor 1 Cause Both Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism</Title>

UL https://suche.suub.uni-bremen.de/peid=jstor-30051458&Exemplar=1&LAN=DE
				
A1 Pitteloud, Nelly
A1 Acierno Jr., James S.
A1 Meysing, Astrid
A1 Eliseenkova, Anna V.
A1 Ma, Jinghong
A1 Ibrahimi, Omar A.
A1 Metzger, Daniel L.
A1 Hayes, Frances J.
A1 Dwyer, Andrew A.
A1 Hughes, Virginia A.
A1 Yialamas, Maria
A1 Hall, Janet E.
A1 Grant, Ellen
A1 Mohammadi, Moosa
A1 Crowley Jr., William F.
PB National Academy of Sciences
YR 2006
SN 0027-8424
K1 normosmia
K1 FGFR1
K1 Biological sciences
K1 Biology
K1 Genetics
K1 Population genetics
K1 Genetic variation
K1 Genetic mutation
K1 Behavioral sciences
K1 Psychology
K1 Cognitive psychology
K1 Perception
K1 Sensory perception
K1 Olfactory perception
K1 Developmental biology
K1 Life cycle
K1 Puberty
K1 Anatomy
K1 Nervous system
K1 Central nervous system
K1 Brain
K1 Olfactory bulb
K1 Phenotypes
K1 Physical sciences
K1 Chemistry
K1 Chemical compounds
K1 Chemicals
K1 Polymers
K1 Biopolymers
K1 Proteins
K1 Receptors
K1 Health sciences
K1 Medical conditions
K1 Diseases
K1 Nervous system diseases
K1 Central nervous system diseases
K1 Neurological disorders
K1 Sensory disorders
K1 Anosmia
K1 Biochemistry
K1 Disorders
K1 Physical disorders
K1 Delayed puberty
K1 Ligands
JF Proceedings of the National Academy of Sciences of the United States of America
VO 103
IS 16
SP 6281
OP 6286
LK http://dx.doi.org/https://www.jstor.org/stable/30051458
DO https://www.jstor.org/stable/30051458
SF ELIB - SuUB Bremen

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