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Journal of Pediatric Endocrinology & Metabolism : JPEM|July 29, 2010
Obesity and reversed growth retardation in a child with type Ia glycogen storage diseaseWikrom Karnsakul, Stacey Gillespie, Kathryn Skitarelic, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 9, 2004
Cleft palate in a newborn with duplication 2(q13q23)Sharon L Wenger, Ona C Bleigh, Marybeth Hummel
Journal of the Association of Genetic Technologists|February 24, 2010
Case report: cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with wolf-hirschhorn syndromeNathanael G Bailey, Sarah T South, Marybeth Hummel, et al.
Prenatal Diagnosis|October 19, 2005
Prenatal detection of deletion 6q13q15 in a complex karyotypeMin Yu, Angela C Obringer, Melissa H Fowler, et al.
American Journal of Medical Genetics. Part A|September 11, 2003
Left-sided CHILD syndrome caused by a nonsense mutation in the NSDHL geneMarybeth Hummel, David Cunningham, Charles J Mullett, et al.
Case Reports in Genetics|October 24, 2013
Persistent mosaicism for 12p duplication/triplication chromosome structural abnormality in peripheral bloodAmy L Shackelford, Laura K Conlin, Marybeth Hummel, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Trisomy 8 mosaicism: selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cellsBonnie J Hulley, Marybeth Hummel, Linda L Cook, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
Molecular and phenotypic characterization of ring chromosome 22Aaron R Jeffries, Sarah Curran, Frances Elmslie, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
Mosaic ring 12p and total anomalous pulmonary venous returnDarren L Harris, Benjamin L Siu, Marybeth Hummel, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndromeSharon L Wenger, Paul D Grossfeld, Benjamin L Siu, et al.
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