المؤلفون: Hammer C; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Pierson S; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Acevedo A; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Goldberg J; Independent (unaffiliated), Washington, District of Columbia, USA., Westover T; Maternal Fetal Medicine and Perinatal Genetics, Capital Health, Trenton, New Jersey, USA., Chawla D; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Mabey B; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Muzzey D; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA., Johansen Taber K; Department of Research & Development, Myriad Genetics, Inc, South San Francisco, California, USA.

المصدر: Prenatal diagnosis [Prenat Diagn] 2024 Jul; Vol. 44 (8), pp. 925-935. Date of Electronic Publication: 2024 Apr 15.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

مواضيع طبية MeSH: DiGeorge Syndrome*/diagnosis , DiGeorge Syndrome*/genetics , Cell-Free Nucleic Acids*/analysis , Cell-Free Nucleic Acids*/blood , Predictive Value of Tests*, Humans ; Female ; Pregnancy ; Adult ; Noninvasive Prenatal Testing/methods ; Noninvasive Prenatal Testing/statistics & numerical data ; Cohort Studies ; Maternal Serum Screening Tests/statistics & numerical data ; Maternal Serum Screening Tests/methods ; Prenatal Diagnosis/methods ; Prenatal Diagnosis/statistics & numerical data

المؤلفون: Palomaki GE; Department of Pathology and Laboratory Medicine, Alpert Medical School at Brown University, Women & Infants Hospital of RI, Providence, Rhode Island, USA., Wyatt P; Esoterix Genetic Laboratories, Santa Fe, New Mexico, USA., Rowsey R; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA., Cacheris PM; Sequenom Laboratories, San Diego, California, USA., Lepage N; Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada., Natowicz MR; Pathology and Laboratory Medicine, Genomic Medicine, Neurology and Pediatrics Institutes, Cleveland Clinic, Cleveland, Ohio, USA., Long T; Department of Biostatistics, College of American Pathologists, Northfield, Illinois, USA., Moyer AM; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.

المصدر: Prenatal diagnosis [Prenat Diagn] 2024 Jul; Vol. 44 (8), pp. 946-952. Date of Electronic Publication: 2024 Apr 15.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

مواضيع طبية MeSH: Cell-Free Nucleic Acids*/analysis , Cell-Free Nucleic Acids*/blood , Noninvasive Prenatal Testing*/methods , Noninvasive Prenatal Testing*/statistics & numerical data, Humans ; Female ; Pregnancy ; Prenatal Diagnosis/methods ; Prenatal Diagnosis/statistics & numerical data ; Trisomy/diagnosis ; Trisomy/genetics ; Maternal Serum Screening Tests/statistics & numerical data ; Maternal Serum Screening Tests/methods

المؤلفون: Zhang M; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Gao Y; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Liang M; Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital, Beijing, 100191, China., Wang Y; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China., Guo L; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Wu D; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Xiao H; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Lin L; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China., Wang H; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China. wanghongdan@zzu.edu.cn.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China. wanghongdan@zzu.edu.cn., Liao S; Medical Genetics Institute of Henan Province, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, 450003, China. ychsgy@126.com.; National Health Commission Key Laboratory of Birth Defects Prevention, Henan Provincial Key Laboratory of Genetic Diseases and Functional Genomics, Zhengzhou, 450003, China. ychsgy@126.com.

المصدر: Archives of gynecology and obstetrics [Arch Gynecol Obstet] 2024 Aug; Vol. 310 (2), pp. 933-942. Date of Electronic Publication: 2024 May 30.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 8710213 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0711 (Electronic) Linking ISSN: 09320067 NLM ISO Abbreviation: Arch Gynecol Obstet Subsets: MEDLINE

مواضيع طبية MeSH: Biomarkers*/blood , DNA Copy Number Variations* , Chorionic Gonadotropin, beta Subunit, Human*/blood , alpha-Fetoproteins*/analysis , alpha-Fetoproteins*/metabolism, Humans ; Female ; Pregnancy ; Retrospective Studies ; Adult ; Pregnancy Trimester, Second/blood ; Estriol/blood ; Comparative Genomic Hybridization ; Chromosome Aberrations ; Karyotyping ; Prenatal Diagnosis/methods ; Maternal Serum Screening Tests

المؤلفون: Dreux S; Biochimie-Hormonologie, Hôpital R. Debré, DMU Biogem AP-HP, Paris, France.; Fédération des CPDPN, Paris, France., Rosenblatt J; Fédération des CPDPN, Paris, France.; Gynécologie-Obstétrique, Hôpital Robert Debré, AP-HP, Paris, France., Massardier J; Fédération des CPDPN, Paris, France.; Gynécologie-Obstétrique, HFME, Hospices Civils de Lyon, Lyon, France.; Centre Français de Référence des Maladies Trophoblastiques, Pierre Bénite, France., Benachi A; Fédération des CPDPN, Paris, France.; Gynécologie-Obstétrique, Hôpital Antoine Béclère, AP-HP, Université Paris Saclay Clamart, Paris, France., Voirin-Mathieu E; Biochimie-Hormonologie, Hôpital R. Debré, DMU Biogem AP-HP, Paris, France., Muller F; Biochimie-Hormonologie, Hôpital R. Debré, DMU Biogem AP-HP, Paris, France.; Fédération des CPDPN, Paris, France.

مؤلفون مشاركون: ABA Study Group

المصدر: Prenatal diagnosis [Prenat Diagn] 2024 Jul; Vol. 44 (8), pp. 959-964. Date of Electronic Publication: 2024 May 17.

نوع المنشور: Journal Article; Multicenter Study

بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

مواضيع طبية MeSH: Down Syndrome*/diagnosis , Down Syndrome*/blood , Down Syndrome*/epidemiology , Chorionic Gonadotropin, beta Subunit, Human*/blood, Humans ; Female ; Pregnancy ; Retrospective Studies ; Adult ; Practice Guidelines as Topic ; Biomarkers/blood ; Prenatal Diagnosis/methods ; Prenatal Diagnosis/statistics & numerical data ; Prenatal Diagnosis/standards ; Maternal Serum Screening Tests/statistics & numerical data

المؤلفون: Zakaria H; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France., Kleinfinger P; Laboratoire Cerba, Saint-Ouen l'Aumône, France., Lohmann L; Laboratoire Cerba, Saint-Ouen l'Aumône, France., Costa JM; Laboratoire Cerba, Saint-Ouen l'Aumône, France., Tsatsaris V; Division of Obstetrics and Gynecology, 'Port Royal' Hospital, Paris Cité University, APHP, Paris, France., Salomon LJ; Division of Obstetrics and Gynecology, 'Necker-Enfants Malades' Hospital, Paris Cité University, APHP, Paris, France., Jouannic JM; Division of Fetal Medicine, 'Armand Trousseau' Hospital, Sorbonne Paris Nord University, APHP, Paris, France., Rosenblatt J; Division of Obstetrics and Gynecology, 'Robert Debré' Hospital, Sorbonne Paris Nord University, APHP, Paris, France., Demain A; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France., Benachi A; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France., El Khattabi L; Non-Invasive Prenatal Screening laboratory, APHP, Paris Cité University, Hôpital Cochin, Paris, France.; Chromosomal Genomics Unit, Medical Genetics Department, APHP, Sorbonne Paris Nord University, Armand Trousseau and Pitié-Salpêtrière Hospitals, Paris, France., Vivanti AJ; Division of Obstetrics and Gynecology, 'Antoine Béclère' Hospital, Paris Saclay University, APHP, Clamart, France.

المصدر: Prenatal diagnosis [Prenat Diagn] 2024 May; Vol. 44 (5), pp. 555-561. Date of Electronic Publication: 2024 Mar 06.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

مواضيع طبية MeSH: Cell-Free Nucleic Acids*/blood , Cell-Free Nucleic Acids*/analysis , Pregnancy, Triplet*, Humans ; Female ; Pregnancy ; Retrospective Studies ; Adult ; Trisomy 18 Syndrome/diagnosis ; Trisomy 18 Syndrome/genetics ; Trisomy 18 Syndrome/blood ; Trisomy/diagnosis ; Trisomy/genetics ; Noninvasive Prenatal Testing/methods ; Noninvasive Prenatal Testing/statistics & numerical data ; Noninvasive Prenatal Testing/standards ; Trisomy 13 Syndrome/diagnosis ; Trisomy 13 Syndrome/blood ; Trisomy 13 Syndrome/genetics ; Cohort Studies ; Down Syndrome/diagnosis ; Down Syndrome/genetics ; Maternal Serum Screening Tests/methods ; Maternal Serum Screening Tests/statistics & numerical data ; Prenatal Diagnosis/methods ; Prenatal Diagnosis/standards

المؤلفون: Texas Education Agency, Austin.

Peer Reviewed: N

Page Count: 21

Descriptors: Check Lists, Exceptional Child Education, Identification, Language Handicaps, Learning Disabilities, Screening Tests

المؤلفون: Texas Education Agency, Austin.

Peer Reviewed: N

Page Count: 359

Descriptors: Competency Based Teacher Education, Elementary School Students, Exceptional Child Education, Exceptional Child Research, Identification, Inservice Teacher Education, Intervention, Language Handicaps, Learning Disabilities, Program Development, Program Effectiveness, Remedial Instruction, Screening Tests

المؤلفون: Norton ME; From the Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, San Francisco.

المصدر: The New England journal of medicine [N Engl J Med] 2022 Oct 06; Vol. 387 (14), pp. 1322-1324. Date of Electronic Publication: 2022 Sep 28.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Massachusetts Medical Society Country of Publication: United States NLM ID: 0255562 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1533-4406 (Electronic) Linking ISSN: 00284793 NLM ISO Abbreviation: N Engl J Med Subsets: MEDLINE

مواضيع طبية MeSH: Cell-Free Nucleic Acids*/blood , Cell-Free Nucleic Acids*/genetics , Chromosome Disorders*/blood , Chromosome Disorders*/diagnosis , Chromosome Disorders*/genetics , Maternal Serum Screening Tests*/methods , Noninvasive Prenatal Testing*/methods , Trisomy*/diagnosis , Trisomy*/genetics, Female ; Humans ; Pregnancy ; Pregnancy Trimester, First ; Prenatal Diagnosis ; Trisomy 13 Syndrome/diagnosis ; Trisomy 13 Syndrome/genetics ; Trisomy 18 Syndrome/diagnosis ; Trisomy 18 Syndrome/genetics

المؤلفون: Centers for Disease Control and Prevention (CDC) (DHHS/PHS)

المصدر: Centers for Disease Control and Prevention. 2024.

Peer Reviewed: N

Page Count: 31

Descriptors: Elementary Secondary Education, Disease Control, Communicable Diseases, Prevention, Microbiology, Health Promotion, Child Health, Hygiene, Immunization Programs, Ventilation, COVID-19, Pandemics, Health Behavior, Sanitation, Screening Tests, Public Health, School Closing, Access to Health Care

المؤلفون: Lauren Koopman (ORCID 0000-0002-5595-793X), Erica Munnik (ORCID 0000-0001-7940-9439), Emma Wagener (ORCID 0000-0002-8846-2327), Mario Smith (ORCID 0000-0002-0281-8290)

المصدر: South African Journal of Education. 2024 44(2).

Peer Reviewed: Y

Page Count: 11

Descriptors: Screening Tests, Emotional Development, Social Development, School Readiness, Test Reliability, Construct Validity, Preschool Children, Interpersonal Competence, Foreign Countries

مصطلحات جغرافية: South Africa