IGNATIA VAN DEN VEYVER to Infant, Newborn
This is a "connection" page, showing publications IGNATIA VAN DEN VEYVER has written about Infant, Newborn.
Connection Strength
0.387
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Lower fetal fraction in clinical cell-free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy. Prenat Diagn. 2022 09; 42(10):1253-1261.
Score: 0.077
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Circulating trophoblast numbers as a potential marker for pregnancy complications. Prenat Diagn. 2022 08; 42(9):1182-1189.
Score: 0.076
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Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes. Am J Med Genet A. 2014 Oct; 164A(10):2633-7.
Score: 0.044
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Management of ornithine transcarbamylase deficiency in pregnancy. Am J Perinatol. 2010 Nov; 27(10):775-84.
Score: 0.033
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Facial and physical features of Aicardi syndrome: infants to teenagers. Am J Med Genet A. 2005 Oct 15; 138A(3):254-8.
Score: 0.024
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Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy. J Child Neurol. 2005 Sep; 20(9):779-83.
Score: 0.024
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Implication of chromosomal microarray analysis prior to in-utero repair of fetal open neural tube defect. Ultrasound Obstet Gynecol. 2023 06; 61(6):719-727.
Score: 0.020
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Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome. Brain Dev. 2001 Dec; 23 Suppl 1:S147-51.
Score: 0.018
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Paralog Studies Augment Gene Discovery: DDX and DHX Genes. Am J Hum Genet. 2019 08 01; 105(2):302-316.
Score: 0.015
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Discordance between fetal RhD typing using molecular methods and neonatal typing with serology. Gynecol Obstet Invest. 1999; 48(4):229-31.
Score: 0.015
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Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn. Am J Obstet Gynecol. 1995 Feb; 172(2 Pt 1):533-40.
Score: 0.011
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Prenatal diagnosis and clinical findings in a case of hexasomy 12p. Am J Med Genet. 1993 Dec 01; 47(8):1171-4.
Score: 0.010
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Antenatal fetal death in twin pregnancies: a dangerous condition mainly for the surviving co-twin; a report of four cases. Eur J Obstet Gynecol Reprod Biol. 1991 Jan 04; 38(1):69-73.
Score: 0.009
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Neuroimaging aspects of Aicardi syndrome. Am J Med Genet A. 2008 Nov 15; 146A(22):2871-8.
Score: 0.007
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Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter. Am J Hum Genet. 2000 Apr; 66(4):1461-4.
Score: 0.004