Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.
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Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene.Next-generation sequencing of patients with congenital anosmia.Isolated GNRH deficiency: genotypic and phenotypic characteristics of the genetically heterogeneous Greek population.Modeling mutant/wild-type interactions to ascertain pathogenicity of PROKR2 missense variants in patients with isolated GnRH deficiency.
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Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on June 2015
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mutation analyses in pedigrees ...... se Kallmann syndrome patients.
@en
Mutation analyses in pedigrees ...... se Kallmann syndrome patients.
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type
label
Mutation analyses in pedigrees ...... se Kallmann syndrome patients.
@en
Mutation analyses in pedigrees ...... se Kallmann syndrome patients.
@nl
prefLabel
Mutation analyses in pedigrees ...... se Kallmann syndrome patients.
@en
Mutation analyses in pedigrees ...... se Kallmann syndrome patients.
@nl
P2093
P2860
P356
P1476
Mutation analyses in pedigrees ...... ese Kallmann syndrome patients
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P2093
An-Ping Wang
Da-Long Zhu
Guang Ning
Guo-Qing Yang
Jian-Ming Ba
Jin-Kui Yang
Jing-Tao Dou
P2860
P304
P356
10.1177/1535370215587531
P50
P577
2015-06-01T00:00:00Z