Effective coding in birth defects surveillance.
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[1] B. Källén,et al. Birth Defects Monitoring Systems , 1984 .
[2] States Services Branch. State birth defects surveillance programs directory, updated May 1999 , 2000 .
[3] M. Cornel,et al. Artefactual increasing frequency of omphaloceles in the Northern Netherlands: lessons for systematic analysis of apparent epidemics. , 1999, International journal of epidemiology.
[4] M. Werler,et al. Predictive value of minor anomalies. I. Association with major malformations. , 1987, The Journal of pediatrics.
[5] E. Zackai,et al. Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects. , 1993, Journal of medical genetics.
[6] F. Jones,et al. International Classification of Diseases , 1978 .
[7] P L Pearson,et al. The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes. , 1997, American journal of medical genetics.
[8] L. Holmes,et al. Anencephaly: Changes in prenatal detection and birth status, 1972 through 1990 , 1994 .
[9] F. Bianchi,et al. Omphalocele and gastroschisis in Europe: a survey of 3 million births 1980-1990. EUROCAT Working Group. , 1995, American journal of medical genetics.
[10] H. Dolk,et al. Registries of congenital anomalies: EUROCAT. , 1993, Environmental health perspectives.
[11] P. De Wals,et al. Prevalence of neural tube defects in the province of Quebec, 1992. , 1999, Canadian journal of public health = Revue canadienne de sante publique.
[12] A. Spira. Epidemiology of human reproduction. , 1986, Human reproduction.
[13] P. Fernhoff,et al. Impact of prenatal diagnosis on the birth prevalence of neural tube defects, Atlanta, 1990-1991. , 1995, Pediatrics.
[14] J D Erickson,et al. Etiologic heterogeneity of neural tube defects: clues from epidemiology. , 1982, American journal of epidemiology.
[15] M. Khoury,et al. The interaction between dysmorphology and epidemiology: methodologic issues of lumping and splitting. , 1992, Teratology.
[16] M. Khoury,et al. Monitoring for multiple congenital anomalies: an international perspective. , 1994, Epidemiologic reviews.
[17] S. L. Murphy,et al. Deaths: final data for 1996. , 1998, National vital statistics reports : from the Centers for Disease Control and Prevention, National Center for Health Statistics, National Vital Statistics System.
[18] T. Crombleholme,et al. Minimal hydronephrosis in the fetus: clinical significance and implications for management. , 1996, The Journal of urology.
[19] A. Ghidini,et al. Clinical outcome of mild fetal ventriculomegaly. , 1998, American journal of obstetrics and gynecology.
[20] R. Kirby,et al. Deaths associated with renal agenesis: a population-based study of birth prevalence, case ascertainment, and etiologic heterogeneity. , 1994, Teratology.
[21] M. Khoury,et al. Interpretation of recurring weak associations obtained from epidemiologic studies of suspected human teratogens. , 1992, Teratology.
[22] H. Hoyme,et al. The vascular pathogenesis of gastroschisis: intrauterine interruption of the omphalomesenteric artery. , 1981, The Journal of pediatrics.
[23] E. Zackai,et al. Frequency of 22q11 deletions in patients with conotruncal defects. , 1998, Journal of the American College of Cardiology.
[24] J. Cordero. Registries of birth defects and genetic diseases. , 1992, Pediatric clinics of North America.
[25] J. Friedman. The use of dysmorphology in birth defects epidemiology. , 1992, Teratology.
[26] M. Khoury,et al. On the use of the term "syndrome" in clinical genetics and birth defects epidemiology. , 1994, American journal of medical genetics.