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A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Hui, Lisa; Poulton, Alice; Kluckow, Eliza; Lindquist, Anthea; Hutchinson, Briohny; Pertile, Mark D; Bonacquisto, Leonard; Gugasyan, Lucy; Kulkarni, Abhijit; Harraway, James; Howden, Amanda; McCoy, Richard; Costa, Fabricio Da Silva; Menezes, Melody; Palma-Dias, Ricardo; Nisbet, Debbie; Martin, Nicole; Bethune, Michael; Poulakis, Zeffie; Halliday, Jane.
Affiliation
  • Hui L; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
  • Poulton A; Department of Obstetrics and Gynaecology, University of Melbourne, Parkville 3052, Victoria, Australia.
  • Kluckow E; Mercy Perinatal, Mercy Hospital for Women, Heidelberg, 3084, Victoria, Australia.
  • Lindquist A; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
  • Hutchinson B; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
  • Pertile MD; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
  • Bonacquisto L; Mercy Perinatal, Mercy Hospital for Women, Heidelberg, 3084, Victoria, Australia.
  • Gugasyan L; Mercy Perinatal, Mercy Hospital for Women, Heidelberg, 3084, Victoria, Australia.
  • Kulkarni A; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
  • Harraway J; Department of Paediatrics, University of Melbourne, Parkville 3052, Victoria, Australia.
  • Howden A; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
  • McCoy R; Cytogenetics, Monash Pathology, Monash Medical Centre, Clayton 3168, Victoria, Australia.
  • Costa FDS; Cytogenetics, Monash Pathology, Monash Medical Centre, Clayton 3168, Victoria, Australia.
  • Menezes M; Department of Cytogenetics/Molecular Pathology, Sullivan Nicolaides Pathology, Bowen Hills, Queensland 4006, Australia.
  • Palma-Dias R; Cytogenetics, Melbourne Pathology, Collingwood 3066, Victoria, Australia.
  • Nisbet D; Molecular Genetics, Australian Clinical Labs, Clayton 3168, Victoria, Australia.
  • Martin N; Department of Gynecology and Obstetrics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14049-900, São Paulo, Brazil.
  • Bethune M; Department of Obstetrics and Gynaecology, Monash University, Clayton 3168, Victoria, Australia.
  • Poulakis Z; Monash Ultrasound for Women, Richmond 3121, Victoria, Australia.
  • Halliday J; Department of Obstetrics and Gynaecology, University of Melbourne, Parkville 3052, Victoria, Australia.
Hum Reprod ; 35(3): 694-704, 2020 03 27.
Article in En | MEDLINE | ID: mdl-32207823
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Aberrations / 22q11 Deletion Syndrome Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adult / Child / Female / Humans / Newborn / Pregnancy Country/Region as subject: Oceania Language: En Journal: Hum Reprod Journal subject: MEDICINA REPRODUTIVA Year: 2020 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Aberrations / 22q11 Deletion Syndrome Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Adult / Child / Female / Humans / Newborn / Pregnancy Country/Region as subject: Oceania Language: En Journal: Hum Reprod Journal subject: MEDICINA REPRODUTIVA Year: 2020 Document type: Article Affiliation country: Country of publication: