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Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.
Semin Perinatol. 2016 Feb;40(1):44-55. doi: 10.1053/j.semperi.2015.11.007. Epub 2015 Dec 21.
Semin Perinatol. 2016.
PMID: 26718445
Free PMC article.
Review.
Whole-exome sequencing for diagnosis of Peters-plus syndrome after prenatal diagnosis of recurrent low PAPP-A and multiple fetal anomalies in two consecutive pregnancies.
Kamalapathy P, Fonda Allen JS, Macri CJ, Lawrence AK, Regier DS, Rubio EI.
Kamalapathy P, et al. Among authors: fonda allen js.
J Neonatal Perinatal Med. 2019;12(3):333-338. doi: 10.3233/NPM-1854.
J Neonatal Perinatal Med. 2019.
PMID: 31476172
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Prenatal diagnosis of Pallister-Killian syndrome: resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization.
McLean S, Stanley W, Stern H, Fonda-Allen J, Devine G, Ellingham T, Rosenbaum K.
McLean S, et al. Among authors: fonda allen j.
Prenat Diagn. 1992 Dec;12(12):985-91. doi: 10.1002/pd.1970121203.
Prenat Diagn. 1992.
PMID: 1287646
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Whole-exome sequencing for diagnosis of Peters-plus syndrome after prenatal diagnosis of recurrent low PAPP-A and multiple fetal anomalies in two consecutive pregnancies.
Kamalapathy P, Fonda Allen JS, Macri CJ, Lawrence AK, Regier DS, Rubio EI.
Kamalapathy P, et al. Among authors: fonda allen js.
J Neonatal Perinatal Med. 2019 May 7. doi: 10.3233/NPM-181854. Online ahead of print.
J Neonatal Perinatal Med. 2019.
PMID: 31081795
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Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysis.
Kashork CD, Sutton VR, Fonda Allen JS, Schmidt DE, Likhite ML, Potocki L, O'Brien WE, Shaffer LG.
Kashork CD, et al. Among authors: fonda allen js.
Prenat Diagn. 2002 Nov;22(11):1028-32. doi: 10.1002/pd.466.
Prenat Diagn. 2002.
PMID: 12424769
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