Prenatal diagnosis of X-linked spinal and bulbar muscular atrophy in a Greek family
- Author
- YAPIJAKIS, C1 ; KAPAKI, E1 ; BOUSSIOU, M; VASSILOPOULOS, D1 ; PAPAGEORGIOU, C1
[1] Department of Neurology, Clinical and Molecular Neurogenetics Unit, University of Athens, Eginition Hospitall, 74 Vas. Sofias, 11528 Athens, Greece - Source
Prenatal diagnosis. 1996, Vol 16, Num 3, pp 262-265 ; ref : 1 p
- CODEN
- PRDIDM
- ISSN
- 0197-3851
- Scientific domain
- Genetics; Obstetrics, gynecology, andrology; General medicine general surgery; Neonatology
- Publisher
- Wiley, Chichester
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Androgène Atrophie Diagnostic Etude familiale Grec Gène Homme Muscle Mutation Neuropathie axone géant Prénatal Récepteur hormonal diagnostic antenatal Hormone stéroïde sexuelle Système nerveux pathologie
- Keyword (en)
- Androgen Atrophia Diagnosis Family study Greek Gene Human Muscle Mutation Giant axonal neuropathy Prenatal Hormonal receptor prenatal diagnosis Sex steroid hormone Nervous system diseases
- Keyword (es)
- Andrógeno Atrofia Diagnóstico Estudio familiar Griego Gen Hombre Músculo Mutación Neuropatía axón gigante Prenatal Receptor hormonal Hormona esteroide sexual Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20F Pregnancy. Fetus. Placenta / 002B20F02 Diseases of mother, fetus and pregnancy
- Discipline
- Gynecology. Andrology. Obstetrics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3050404
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/(SICI)1097-0223(199603)16:3<262::AID-PD841>3.0.CO;2-F 
https://dx.doi.org/10.1002/(SICI)1097-0223(199603)16:3<262::AID-PD841>3.0.CO;2-F
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