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Clinical Dysmorphology|June 7, 2007
Further delineation of interstitial chromosome 6 deletion syndrome and review of the literatureMonica M Zherebtsov, Rachel T Klein, Hana Aviv, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: a case seriesNaomi Yachelevich, Julia Klein Gittler, Susan Klugman, et al.
American Journal of Medical Genetics. Part A|August 9, 2018
Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCNRachel D Burnside, Sharon Molinari, Christina Botti, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|February 19, 2005
Prenatal diagnostic testing for infantile and late-infantile neuronal ceroid lipofusinoses (NCL) using allele specific primer extension (ASPE)Nanbert Zhong, Weina Ju, Dorota Moroziewicz, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Medium chain acyl-CoA dehydrogenase deficiency detected among Hispanics by New Jersey newborn screeningSharon Anderson, Christina Botti, Bo Li, et al.
Work (Reading, Mass.)|June 13, 2022
Why serendipitous informal knowledge sharing interactions are key to boundary spanning and creativityPhilip Roth
The Journal of Craniofacial Surgery|May 26, 2012
Apert syndrome in a newborn infant without craniosynostosisSivaroopi Coomaralingam, Philip Roth
Pediatrics in Review|December 31, 2022
Early-Onset Sepsis in NewbornsCourtney Briggs-Steinberg, Philip Roth
Neurobiology of Aging|July 28, 2005
Telomere shortening in T lymphocytes of older individuals with Down syndrome and dementiaEdmund C Jenkins, Milen T Velinov, Lingling Ye, et al.
Breastfeeding Medicine : the Official Journal of the Academy of Breastfeeding Medicine|March 31, 2016
Factors Associated with Supplemental Formula Feeding of Breastfeeding Infants During Postpartum Hospital StayJoanna Pierro, Bdair Abulaimoun, Philip Roth, et al.
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