Karyotype, phenotype and parental origin in 19 cases of triploidy
- Author
- DANIEL, Art1 ; ZHANHE WU1 ; LOO, Christine8 ; BENNETTS, Bruce2 ; SLATER, Howard3 ; OSBORN, Robert4 ; JACKSON, Julianne2 ; PUPKO, Vladimir3 ; NELSON, John5 ; WATSON, Geoff6 ; COOKE-YARBOROUGH, Claire7
[1] Department of Cytogenetics, The Children's Hospital at Westmead, NSW 2145, Australia
[2] Department of Molecular Genetics, The Children's Hospital at Westmead, NSW 2145, Australia
[3] Department of Cytogenetics, Royal Children's Hospital, Murdoch Institute, Parkville, VIC 3052, Australia
[4] Department of Anatomical Pathology, ICPMR, Westmead Hospital, Westmead, NSW 2145, Australia
[5] Department of Clinical Genetics, King Edvard Memorial Hospital, Subiaco, WA 6008, Australia
[6] Department of Anatomical Pathology, Royal Prince Alfred Hospital, Camperdown, NSW 2050, Australia
[7] Department of Histopathology, The Children's Hospital at Westmead, NSW 2145, Australia
[8] Department of Anatomical Pathology, Liverpool Hospital, NSW 2170, Australia - Source
Prenatal diagnosis. 2001, Vol 21, Num 12, pp 1034-1048 ; ref : 26 ref
- 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)
- Avortement Caryotype DNA microsatellite Diagnostic Diploïdie Etude cas Foetus Homme Origine parentale Parent Pathogénie Phénotype Précoce Prénatal Réaction chaîne polymérase Triploïdie Diandrie Digynie Aberration chromosomique Biologie moléculaire Cytogénétique Gestation pathologie Maladie congénitale
- Keyword (en)
- Abortion Karyotype Microsatellite DNA Diagnosis Diploidy Case study Fetus Human Parental origin Parent Pathogenesis Phenotype Early Prenatal Polymerase chain reaction Triploidy Chromosomal aberration Molecular biology Cytogenetics Pregnancy disorders Congenital disease
- Keyword (es)
- Aborto Cariotipo DNA microsatélite Diagnóstico Diploidía Estudio caso Feto Hombre Origen parental Pariente Patogenia Fenotipo Precoz Prenatal Reacción cadena polimerasa Triploidía Aberración cromosómica Biología molecular Citogenética Gestación patología Enfermedad congénita
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B20 Gynecology. Andrology. Obstetrics / 002B20A Birth control / 002B20A04 Sterility. Assisted procreation
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations
- Discipline
- Gynecology. Andrology. Obstetrics Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 13794290
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
Access to the document
Install on your browser
DOI
10.1002/pd.164 
https://dx.doi.org/10.1002/pd.164
"O:13:\"PanistOpenUrl\":36:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000idc\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1002\/pd.164\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:9:\"\u0000*\u0000jtitle\";s:18:\"Prenatal diagnosis\";s:9:\"\u0000*\u0000stitle\";s:13:\"Prenat. diagn\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:2:\"21\";s:8:\"\u0000*\u0000issue\";s:2:\"12\";s:8:\"\u0000*\u0000spage\";s:4:\"1034\";s:8:\"\u0000*\u0000epage\";s:4:\"1048\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0197-3851\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"DANIEL\";s:10:\"\u0000*\u0000aufirst\";s:3:\"Art\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:10:{i:0;s:9:\"ZHANHE WU\";i:1;s:14:\"LOO, Christine\";i:2;s:15:\"BENNETTS, Bruce\";i:3;s:14:\"SLATER, Howard\";i:4;s:14:\"OSBORN, Robert\";i:5;s:17:\"JACKSON, Julianne\";i:6;s:15:\"PUPKO, Vladimir\";i:7;s:12:\"NELSON, John\";i:8;s:13:\"WATSON, Geoff\";i:9;s:24:\"COOKE-YARBOROUGH, Claire\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"PRDIDM\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Panist access
"O:12:\"IstexOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1002\/pd.164\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:9:\"\u0000*\u0000jtitle\";s:18:\"Prenatal diagnosis\";s:9:\"\u0000*\u0000stitle\";s:13:\"Prenat. diagn\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:2:\"21\";s:8:\"\u0000*\u0000issue\";s:2:\"12\";s:8:\"\u0000*\u0000spage\";s:4:\"1034\";s:8:\"\u0000*\u0000epage\";s:4:\"1048\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0197-3851\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"DANIEL\";s:10:\"\u0000*\u0000aufirst\";s:3:\"Art\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:10:{i:0;s:9:\"ZHANHE WU\";i:1;s:14:\"LOO, Christine\";i:2;s:15:\"BENNETTS, Bruce\";i:3;s:14:\"SLATER, Howard\";i:4;s:14:\"OSBORN, Robert\";i:5;s:17:\"JACKSON, Julianne\";i:6;s:15:\"PUPKO, Vladimir\";i:7;s:12:\"NELSON, John\";i:8;s:13:\"WATSON, Geoff\";i:9;s:24:\"COOKE-YARBOROUGH, Claire\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"PRDIDM\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Istex access
"O:16:\"UnpaywallOpenUrl\":35:{s:8:\"\u0000*\u0000email\";s:27:\"assistance-portail@inist.fr\";s:6:\"\u0000*\u0000fmt\";N;s:6:\"\u0000*\u0000doi\";s:14:\"10.1002\/pd.164\";s:6:\"\u0000*\u0000pii\";N;s:7:\"\u0000*\u0000pmid\";N;s:9:\"\u0000*\u0000atitle\";N;s:9:\"\u0000*\u0000jtitle\";N;s:9:\"\u0000*\u0000stitle\";N;s:7:\"\u0000*\u0000date\";N;s:9:\"\u0000*\u0000volume\";N;s:8:\"\u0000*\u0000issue\";N;s:8:\"\u0000*\u0000spage\";N;s:8:\"\u0000*\u0000epage\";N;s:8:\"\u0000*\u0000pages\";N;s:7:\"\u0000*\u0000issn\";N;s:8:\"\u0000*\u0000eissn\";N;s:9:\"\u0000*\u0000aulast\";N;s:10:\"\u0000*\u0000aufirst\";N;s:9:\"\u0000*\u0000auinit\";N;s:10:\"\u0000*\u0000auinitm\";N;s:5:\"\u0000*\u0000au\";N;s:9:\"\u0000*\u0000aucorp\";N;s:7:\"\u0000*\u0000isbn\";N;s:8:\"\u0000*\u0000coden\";N;s:8:\"\u0000*\u0000genre\";N;s:7:\"\u0000*\u0000part\";N;s:9:\"\u0000*\u0000btitle\";N;s:8:\"\u0000*\u0000title\";N;s:8:\"\u0000*\u0000place\";N;s:6:\"\u0000*\u0000pub\";N;s:10:\"\u0000*\u0000edition\";N;s:9:\"\u0000*\u0000tpages\";N;s:9:\"\u0000*\u0000series\";N;s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";N;}"
Unpaywall access
"O:16:\"EuropePMCOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1002\/pd.164\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:9:\"\u0000*\u0000jtitle\";s:18:\"Prenatal diagnosis\";s:9:\"\u0000*\u0000stitle\";s:13:\"Prenat. diagn\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:2:\"21\";s:8:\"\u0000*\u0000issue\";s:2:\"12\";s:8:\"\u0000*\u0000spage\";s:4:\"1034\";s:8:\"\u0000*\u0000epage\";s:4:\"1048\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0197-3851\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"DANIEL\";s:10:\"\u0000*\u0000aufirst\";s:3:\"Art\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:10:{i:0;s:9:\"ZHANHE WU\";i:1;s:14:\"LOO, Christine\";i:2;s:15:\"BENNETTS, Bruce\";i:3;s:14:\"SLATER, Howard\";i:4;s:14:\"OSBORN, Robert\";i:5;s:17:\"JACKSON, Julianne\";i:6;s:15:\"PUPKO, Vladimir\";i:7;s:12:\"NELSON, John\";i:8;s:13:\"WATSON, Geoff\";i:9;s:24:\"COOKE-YARBOROUGH, Claire\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"PRDIDM\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Europe PubMed Central access
"O:11:\"BaseOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1002\/pd.164\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:9:\"\u0000*\u0000jtitle\";s:18:\"Prenatal diagnosis\";s:9:\"\u0000*\u0000stitle\";s:13:\"Prenat. diagn\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:2:\"21\";s:8:\"\u0000*\u0000issue\";s:2:\"12\";s:8:\"\u0000*\u0000spage\";s:4:\"1034\";s:8:\"\u0000*\u0000epage\";s:4:\"1048\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0197-3851\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"DANIEL\";s:10:\"\u0000*\u0000aufirst\";s:3:\"Art\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:10:{i:0;s:9:\"ZHANHE WU\";i:1;s:14:\"LOO, Christine\";i:2;s:15:\"BENNETTS, Bruce\";i:3;s:14:\"SLATER, Howard\";i:4;s:14:\"OSBORN, Robert\";i:5;s:17:\"JACKSON, Julianne\";i:6;s:15:\"PUPKO, Vladimir\";i:7;s:12:\"NELSON, John\";i:8;s:13:\"WATSON, Geoff\";i:9;s:24:\"COOKE-YARBOROUGH, Claire\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"PRDIDM\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Base Search access
"O:12:\"ArXivOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1002\/pd.164\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:9:\"\u0000*\u0000jtitle\";s:18:\"Prenatal diagnosis\";s:9:\"\u0000*\u0000stitle\";s:13:\"Prenat. diagn\";s:7:\"\u0000*\u0000date\";s:4:\"2001\";s:9:\"\u0000*\u0000volume\";s:2:\"21\";s:8:\"\u0000*\u0000issue\";s:2:\"12\";s:8:\"\u0000*\u0000spage\";s:4:\"1034\";s:8:\"\u0000*\u0000epage\";s:4:\"1048\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"0197-3851\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:6:\"DANIEL\";s:10:\"\u0000*\u0000aufirst\";s:3:\"Art\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:10:{i:0;s:9:\"ZHANHE WU\";i:1;s:14:\"LOO, Christine\";i:2;s:15:\"BENNETTS, Bruce\";i:3;s:14:\"SLATER, Howard\";i:4;s:14:\"OSBORN, Robert\";i:5;s:17:\"JACKSON, Julianne\";i:6;s:15:\"PUPKO, Vladimir\";i:7;s:12:\"NELSON, John\";i:8;s:13:\"WATSON, Geoff\";i:9;s:24:\"COOKE-YARBOROUGH, Claire\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"PRDIDM\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:65:\"Karyotype, phenotype and parental origin in 19 cases of triploidy\";s:8:\"\u0000*\u0000place\";s:10:\"Chichester\";s:6:\"\u0000*\u0000pub\";s:5:\"Wiley\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:0:\"\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
arXiv access
