Rhonda Spiro

Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism

C. E. Jones, Carol Booth, Debra Rita et al. · Prenatal Diagnosis · 1995 · 98 citations

Two 22q telomere deletions serendipitously detected by FISH.

Kathrin S. Precht, Christa M. Lese, Rhonda Spiro et al. · Journal of Medical Genetics · 1998 · 82 citations · Full text

Biology, Developmental Biology, Mendelian Disorder +13

Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p

Xueya Hauge, Gordana Raca, S. F. Cooper et al. · Genetics in Medicine · 2008 · 67 citations · Full text

Chromatin, Detailed Characterization, Cytogenetics +10

Using three‐dimensional ultrasound to detect craniosynostosis in a fetus with Pfeiffer syndrome

Beryl R. Benacerraf, Rhonda Spiro, Amanda Mitchell · Ultrasound in Obstetrics and Gynecology · 2000 · 64 citations

Significance of genetic testing for paternal uniparental disomy of chromosome 6 in neonatal diabetes mellitus

Susan L. Christian, Barry H. Rich, Charli Loebl et al. · The Journal of Pediatrics · 1999 · 46 citations

Genetic Testing, Developmental Biology, Prenatal Genetic Testing +11