Reproductive and Child Health
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Records 1 - 30 (of 388 Records) |
| Query Trace: Birth Defects Or Congenital Anomalies[original query]>>Reviews/Commentaries[Product Type] |
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| Genetics of diaphragmatic hernia. Schreiner Yannick et al. European journal of human genetics : EJHG 2021 |
| Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist. Mancini Grazia M S et al. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2021 3527-34 |
| Perinatal health predictors using artificial intelligence: A review. Ramakrishnan Rema et al. Women's health (London, England) 2021 1717455065211046132 |
| Clinical trials in skeletal dysplasia: a paradigm for treating rare diseases. Sabir Ataf et al. British medical bulletin 2021 |
| From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns. Zhytnik Lidiia et al. Human reproduction update 2021 |
| Genomic frontiers in congenital heart disease. Morton Sarah U et al. Nature reviews. Cardiology 2021 |
| Ethical implications of next-generation sequencing and the future of newborn screening. White-Corey Shelley et al. Journal of the American Association of Nurse Practitioners 2021 33(7) 492-495 |
| [Experience and lessons on guiding and governing clinical applications of chromosome microarray analysis in the United States]. Xie Xiaolei et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 38(5) 419-424 |
| Understanding Pregnancy Loss, Infertility, Birth Defects and the MTHFR gene: What Everyone Should Know J Gunter, the Vajenda, March 27, 2021 |
| World Birth Defects Day, March 3, 2021 CDC, March 2021 |
| Birth Defects Surveillance Readiness Assessment Tool Public Health Informatics Institute, February 2021 |
| Webinar: Launch of new birth defects surveillance toolkit - December 2nd, 2020, 9AM EST Join the World Health Organization (WHO), the Centers for Disease Control and Prevention (CDC), and the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR) at a virtual event to launch the new toolkit - Birth defects surveillance: a manual for programme managers and Birth defects surveillance: quick reference handbook of selected congenital anomalies. |
| Unlocking the genetic complexity of congenital hydrocephalus ME Ross, Nature Medicine, October 26, 2020 |
| Optimizing Genetic Diagnosis of Neurodevelopmental Disorders in the Clinical Setting. Michelson David Joshua et al. Clinics in laboratory medicine 2020 Sep 40(3) 231-256 |
| Non-invasive prenatal testing: A diagnostic innovation shaped by commercial interests and the regulation conundrum. Löwy Ilana et al. Social science & medicine (1982) 2020 May 113064 |
| Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract. Westland Rik et al. Clinical journal of the American Society of Nephrology : CJASN 2020 Apr |
| [When is it necessary to refer a child with cancer to genetic counseling?] Ripszám Réka et al. Magyar onkologia 2020 Mar 64(1) 38-42 |
| [Fathoming of NIPT to further improve the efficiency of prenatal screening for birth defects]. Hu Y L et al. Zhonghua fu chan ke za zhi 2020 Feb 55(2) 91-93 |
| The de-coders: A historical perspective of the genetic counseling profession. Cohen Leslie et al. Birth defects research 2020 Mar 112(4) 307-315 |
| Mandatory newborn screening in the United States: History, current status, and existential challenges. McCandless Shawn E et al. Birth defects research 2020 Mar 112(4) 350-366 |
| Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects. Berisha Stela Z et al. Birth defects research 2020 Mar 112(4) 293-306 |
| Is preparation a good reason for prenatal genetic testing? Ethical and critical questions. Michie Marsha et al. Birth defects research 2020 Mar 112(4) 332-338 |
| Fertility preservation in BRCA mutation carriers-efficacy and safety issues: a review. Zhang Xiaofu et al. Reproductive biology and endocrinology : RB&E 2020 Feb 18(1) 11 |
| Introduction to the special issue on "Genetic Screening and Testing". Mitchell Anna L et al. Birth defects research 2020 Feb |
| Genetic Testing in Pediatric Kidney Disease. Arora Veronica et al. Indian journal of pediatrics 2020 Feb |
| Genetic counseling for fetal gastrointestinal anomalies. Schindewolf Erica et al. Current opinion in obstetrics & gynecology 2020 Feb |
| Genetics of Congenital Heart Disease. Williams Kylia et al. Biomolecules 2019 Dec 9(12) |
| Helping Children Live to the Fullest by Understanding Developmental Disabilities, National Center on Birth Defects and Developmental Disabilities (NCBDDD), CDC |
| Saving Babies Through Surveillance, Research, and Prevention of Birth Defects and Infant Disorders, National Center on Birth Defects and Developmental Disabilities (NCBDDD), CDC |
| Genome-wide association studies of structural birth defects: A review and commentary. Lupo Philip J et al. Birth defects research 2019 Oct |