Fetus with Casamassima-Morton-Nance syndrome and an inherited (6;9) balanced translocation
- Author
- DAÏKHA-DAHMANE, F1 ; HUTEN, Y1 ; MORVAN, J2 ; SZPIRO-TAPIA, S3 ; NESSMANN, C1 ; EYDOUX, P1
[1] Service de Biologie du Développement, Hôpital Robert-Debré, Paris, France
[2] Maternité, Hôpital de Montmorency, Montmorency, France
[3] CERBA, Cergy-Pontoise, France - Source
American journal of medical genetics. = Neuropsychiatric genetics. 1998, Vol 80, Num 5, pp 514-517 ; ref : 5 ref
- Publisher
- Wiley-Liss, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Appareil urogénital Association Chromosome C6 anormal Chromosome C9 anormal Dysmorphie faciale Etude cas Foetus Homme Jarcho Levin syndrome Malformation Paroi thoracique Phénotype Thorax Translocation chromosomique Casamassima Norton Nance syndrome Aberration chromosomique Chromosome anormal Génétique Maladie héréditaire Stomatologie Syndrome complexe Système ostéoarticulaire pathologie
- Keyword (en)
- Urogenital system Association Abnormal chromosome C6 Abnormal chromosome C9 Dysmorphic facies Case study Fetus Human Jarcho Levin syndrome Malformation Chest wall Phenotype Thorax Chromosome translocation Casamassima Norton Nance syndrome Chromosomal aberration Abnormal chromosome Genetics Genetic disease Stomatology Complex syndrome Diseases of the osteoarticular system
- Keyword (es)
- Aparato urogenital Asociación Cromosoma C6 anormal Cromosoma C9 anormal Dismorfia facial Estudio caso Feto Hombre Jarcho Levin síndrome Malformación Pared torácica Fenotipo Tórax Translocación cromosómica Aberración cromosómica Cromosoma anormal Genética Enfermedad hereditaria Estomatología Síndrome complejo Sistema osteoarticular patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23E Complex syndromes
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1615039
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)1096-8628(19981228)80:5<514::AID-AJMG15>3.0.CO;2-0 
https://dx.doi.org/10.1002/(SICI)1096-8628(19981228)80:5<514::AID-AJMG15>3.0.CO;2-0
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