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1 Ergebnisse
1
A recessive PRDM13 mutation results in congenital hypogonad..:
Whittaker D. E
;
Oleari R
;
Gregory L. C
...
info:eu-repo/semantics/altIdentifier/pmid/34730112. , 2021
Link:
http://hdl.handle.net/2434/904933
RT Journal T1
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
UL https://suche.suub.uni-bremen.de/peid=base-ftunivmilanoair:oai:air.unimi.it:2434_904933&Exemplar=1&LAN=DE A1 Whittaker D. E A1 Oleari R A1 Gregory L. C A1 Le Quesne-Stabej P A1 Williams H. J A1 Torpiano J. G A1 Formosa N A1 Cachia M. J A1 Field D A1 Lettieri A A1 Ocaka L. A A1 Paganoni A. J. J A1 Rajabali S. H A1 Riegman K. L. H A1 de Martini L. B A1 Chaya T A1 Robinson I. C. A. F A1 Furukawa T A1 Cariboni A A1 Basson M. A A1 Dattani M. T PB American Society for Clinical Investigation YR 2021 K1 Development K1 Endocrinology K1 Genetic disease K1 Neurodevelopment K1 Neuroendocrine regulation K1 Animal K1 Cerebellum K1 Developmental Disabilitie K1 Disease Models K1 Human K1 Hypothalamu K1 Mice K1 Mutant Strain K1 Neuron K1 Histone-Lysine N-Methyltransferase K1 Hypogonadism K1 Mutation K1 Nervous System Malformation K1 Transcription Factors K1 Settore BIO/13 - Biologia Applicata JF info:eu-repo/semantics/altIdentifier/pmid/34730112 LK http://hdl.handle.net/2434/904933 DO http://hdl.handle.net/2434/904933 SF ELIB - SuUB Bremen
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