Erratum: Pregnancy outcome of fetuses with trisomy 18 identified by prenatal sonography and chromosomal analysis in a perinatal center (American Journal of Medical Genetics DOI: 10.1002/ajmg.a.31241);Pregnancy outcome of fetuses with trisomy 18 identified by prenatal sonography and chromosomal analysis in a perinatal center

American Journal of Medical Genetics, Part A

Volumn 140, Issue 11, 2006, Pages 1177-1182

  Yamanaka, Michiko ^a   Setoyama, Takuya ^a   Igarashi, Youko ^a   Kurosawa, Kenji ^a   Itani, Yasufumi ^a   Hashimoto, Sakae ^a   Saitoh, Keisuke ^a   Takei, Miki ^a   Hirabuki, Tomoo ^a  

^a KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

Author keywords

Natural history; Prenatal diagnosis; Trisomy 18

Indexed keywords

ARTICLE; CESAREAN SECTION; CHROMOSOME ANALYSIS; COUNSELING; FEMALE; FETUS; FETUS DEATH; FETUS OUTCOME; GESTATIONAL AGE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MEDICAL DECISION MAKING; PREGNANCY OUTCOME; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; SEX RATIO; SURVIVAL TIME; TRISOMY 18;

EID: 33744803233     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/aimg.a.31356     Document Type: Erratum

References (14)

1. Baty BJ, Blackburn BL, Carey JC. 1994. Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence risk. Am J Med Genet 49:175-188,
2. Benacerraf BR. 2000. Ultrasound evaluation of chromosomal abnormalities. In: Callen PW, editor. Ultrasonography in obstetrics and gynecology. 4th edn. Philadelphia: WB Saunders. 57p.
3. Carothers AD, Boyd E, Lowther G, Ellis PM, Couzin DA, Faed MJ, Robb A. 1999. Trends in prenatal diagnosis of Down Syndrome and other autosomal trisomies in Scotland 1990-1994, with associated cytogenetic and epidemiological findings. Genet Epidemiol 16:179-190.
4. Carter PE, Pearn JH, Bell J, Martin N, Anderson NG. 1985. Survival in trisomy 18. Life tables for use in genetic counselling and clinical paediatrics. Clin Genet 27:59-61.
5. Embleton ND, Wyllie JP, Wright MJ, Burn J, Hunter S. 1996. Natural history of trisomy 18. Arch Dis Child Fetal Neonatal Ed 75:F38-F41.
6. Hook EB, Topol BB, Cross PK, 1989. The natural history of cytogenetically abnormal fetuses detected at midtrimester amniocentesis which are not terminated electively: New data and estimates of the excess and relative risk of late fetal death associated with 47,+21 and some other abnormal karyotypes. Am J Hum Genet 45:855-861.
7. Japan Association of Obstetrician and Gynecologists. 1993-2004. The annual report of congenital malformations of 1993(for each year to 2004).
8. Jones KL, Smith DW. 1996. Smith's recognizable patterns of human malformation. 5th edn. Philadelphia: W B Saunders Co. 14p.
9. Kuroki Y, Kurosawa K. 2004. No sex differences in 18 trisomy births in the Kanagawa Birth Defects Monitoring Program. Congenit Anom 44:97-98.
10. Parker MJ, Budd JLS, Draper ES, Young ID. 2003. Trisomy 13 and trisomy 18 in a defined population: Epidemiological, genetic and prenatal observations. Prenat Diagn 23:856-860.
11. Press N, Browner CH. 1998. Characteristics of women who refuse an offer of prenatal diagnosis: Data from the California maternal serum alpha fetoprotein blood test experience. Am J Med Genet 78:433-445.
12. Root S, Carey JC. 1994. Survival in trisomy 18. Am J Med Genet 49: 170-174
13. Sago H, Suzumori K, Uehara S, Okuyama K, Miharu N, Tanemura M, Yamanaka M, Hirahara F. 2005. Trends of Prenatal Diagnosis in Japan (1998-2002). J Jpn Soc Perinat Neonat Med 41:561-654.
14. Won RH, Currier RJ, Lorey F, Towner DR. 2005. The timing of demise in fetuses with trisomy 21 and trisomy 18. Prenat Diagn 25:608-611.