Thomas Jefferson University

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Donnenfeld, Alan
One or more keywords matched the following items that are connected to Donnenfeld, Alan
Item TypeName
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 14
Concept Chromosomes, Human, Pair 18
Concept Chromosomes, Human, Pair 20
Concept Chromosomes, Human, Pair 21
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Y
Academic Article Mosaic paternal uniparental (iso)disomy for chromosome 20 associated with multiple anomalies.
Academic Article Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency.
Academic Article Fetal pyelectasis: does fetal gender modify the risk of major trisomies?
Academic Article Complete trisomy 21 vs translocation Down syndrome: a comparison of modes of ascertainment.
Academic Article Prenatal diagnosis of a jumping translocation.
Academic Article Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion.
Academic Article Trizygotic dichorionic triplets with 46,XX/46,XY chimerism in both fetuses of the monochorionic pair.
Academic Article Risk and benefit analysis of offering karyotyping for an isolated choroid plexus cyst.
Academic Article Sonographic findings in fetuses with common chromosome abnormalities.
Academic Article Molecular characterization of de novo secondary trisomy 13.
Academic Article Trisomy 20 mosaicism in amniotic fluid culture.
Academic Article Prenatal sonographic detection of isolated fetal choroid plexus cysts: should we screen for trisomy 18?
Academic Article A second report of normal outcome with mosaic isochromosome 20q found on amniocentesis.
Academic Article Significance of mosaic isochromosome 20q on amniocentesis.
Academic Article De novo 2q+ masquerading as Smith-Lemli-Opitz syndrome.
Academic Article Prenatal diagnosis of the derivative chromosome 22 associated with cat eye syndrome by fluorescence in situ hybridization.
Academic Article Microphthalmia and chorioretinal lesions in a girl with an Xp22.2-pter deletion and partial 3p trisomy: clinical observations relevant to Aicardi syndrome gene localization.
Academic Article De novo inverted interstitial ("mirror") duplication of chromosome 8(q13----q24.1) in a liveborn male.
Academic Article Tissue-specific mosaicism among fetuses with prenatally diagnosed diaphragmatic hernia.
Academic Article Clinical, cytogenetic, and pedigree findings in 18 cases of Aicardi syndrome.
Search Criteria
  • Chromosomes Human