Results 321 to 330 of about 1,997,745 (357)
Some of the next articles are maybe not open access.

Prenatal Screening and Diagnosis for Pediatricians

Pediatrics, 2004
This Technical Report was retired January 2011. The pediatrician who cares for a child with a birth defect or genetic disorder may be in the best position to alert the family to the possibility of a recurrence of the same or similar problems in future offspring.
openaire   +2 more sources

Prenatal Carrier Screening

JAMA, 2016
Imran S, Haque   +2 more
openaire   +2 more sources

Prenatal diagnosis and screening of the haemoglobinopathies.

Bailliere's clinical haematology, 2000
This paper reviews the most important aspects of carrier detection procedures, genetic counselling, population screening and prenatal diagnosis of the thalassaemias and sickle cell anaemia. Carrier detection can be made retrospectively, following the birth of an affected child, or prospectively.
Antonio, Cao   +2 more
openaire   +2 more sources

Prospective prenatal cell-free DNA screening for genetic conditions of heterogenous etiologies

Nature Medicine
Jinglan Zhang   +29 more
semanticscholar   +1 more source

Heterogeneity in prenatal substance use screening despite universal screening recommendations: findings from PRAMS, 2016-2018.

American Journal of Obstetrics & Gynecology MFM, 2021
Esita Patel   +8 more
semanticscholar   +1 more source

Prenatal diagnosis and screening

International Journal of Gynecology & Obstetrics, 2012
openaire   +2 more sources

Screening in prenatal diagnosis

International Journal of Risk and Safety in Medicine, 1990
openaire   +2 more sources

Current landscape of prenatal genetic screening and testing

Birth Defects Research, 2020
Nevena Krstić, Sarah G Običan
exaly  

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