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020 _a9789811581717
024 7 _a10.1007/978-981-15-8171-7
_2doi
040 _bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aRG628
_b2021 EB
245 0 0 _aFetal Morph Functional Diagnosis
_cedited by Hideaki Masuzaki
250 _a1st edition 2021
264 1 _aSingapore
_bSpringer International Publishing
_c2021
300 _a1 recurso en línea (IX, 354 páginas)
_b108 ilustraciones, 60 ilustraciones a color
336 _2rdacontent
_aTexto
_btxt
337 _2rdamedia
_aelectrónico
_bc
338 _2rdacarrier
_arecurso electrónico
_bcr
347 _aarchivo de texto
_bPDF
490 0 _aComprehensive Gynecology and Obstetrics
_x2364-219X
505 0 _aPart I Ultrasound examination -- 1.Ultrasonic Screenin -- 2.Abnormal findings in Ultrasound examination -- Part II_ Genetic tests -- 3.Screening tests -- 4.Diagnostic test -- Part III_Genetic Disorders -- 5.Mendelian Diseases -- 6.Abnormalities in fetal brain(congenital hydrocephalus etc) -- 7.Muscular Dystrophy -- 8.Skeletal dysplasia -- 9.Genito-urinary tract abnormality -- 10.Genomic imprinting disorders ( including mesenchymal placental dysplasia) -- 11.Genetics in Multiple gestation -- 12.Fetal Therapy -- Part IV_Chromosoma disease -- 13.Autosomal disease -- 14.Sex chromosome-linked diseases -- Part V_Genetic counseling -- 15.fetal anomaly and genetic counseling -- 16.Soft marker test (NT, Nasal bone etc) and genetic counseling -- 17.NIPT and genetic counseling -- 18.Trisomy and genetic counseling -- 19.Sex chromosomel abnormality and genetic counseling -- 20.Chromosome structural abnormalities and genetic counseling -- 21.Chromosome Mosaic and Genetic Counseling -- 22.Gene disorders and genetic counseling -- Part VI_Technical -- 23. G-banding -- 24. FISH -- 25. PCR -- 26. Microarray and Next generation sequencing -- 27. How to get the licenses for prenatal diagnosis.
520 3 _aThis book explores the recent clinical and research findings in the field of prenatal screening and diagnosis. It presents new devices and tests such as real-time 3D ultrasound, ultrafast fetal MRI, and next-generation sequencing and discusses genetic counseling and fetal therapy. Written by pioneering scientists, the book is divided into six themed parts: ultrasound examination, genetic tests, genetic disorders, chromosomal diseases, genetic counseling, and techniques, presenting carefully prepared original data.This thought-provoking, instructive and informative book is intended for geneticists, obstetricians, pediatricians, genetic counselors and nurses. Although the incidence of congenital abnormalities such as structural, chromosomal and genetic disorders is very low, it is important to have accurate information on their incidence and likely outcome, and on the screening and diagnosis of congenital abnormalities during pregnancy care. This book provides valuable insights into prenatal screening, genetic counseling and fetal diagnosis.
988 _aSpringer_Medicine_2021
650 7 _2embne
_9140759
_aDiagnóstico prenatal
700 1 _aMasuzaki, Hideaki
_eeditor literario
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
776 0 8 _iPrinted edition:
_z9789811581700
776 0 8 _iPrinted edition:
_z9789811581724
776 0 8 _iPrinted edition:
_z9789811581731
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-981-15-8171-7
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
998 _b11/2022
_dz
_eu
_zSI