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American Journal of Medical Genetics. Part A|November 16, 2007
A study of 534 fetal pathology cases from prenatal diagnosis referrals analyzed from 1989 through 2000Anna Laury, Pedro A Sanchez-Lara, Samuel Pepkowitz, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 4, 2019
Approach to overgrowth syndromes in the genome eraDeepika D Burkardt, Katrina Tatton-Brown, William Dobyns, et al.Clinical Pediatrics|February 19, 2004
22q13 deletion syndrome: an update and review for the primary pediatricianJoaquim M Havens, Jeannie Visootsak, Mary C Phelan, et al.American Journal of Medical Genetics. Part A|January 8, 2005
CHARGE syndrome from birth to adulthood: an individual reported on from 0 to 33 yearsLisa C Searle, John M Graham, Chitra Prasad, et al.American Journal of Medical Genetics. Part A|May 15, 2007
Behavioral phenotype of sex chromosome aneuploidies: 48,XXYY, 48,XXXY, and 49,XXXXYJeannie Visootsak, Beth Rosner, Elisabeth Dykens, et al.Journal of Pregnancy|August 14, 2012
Extrinsic factors influencing fetal deformations and intrauterine growth restrictionWendy Moh, John M Graham, Isha Wadhawan, et al.American Journal of Medical Genetics. Part A|July 3, 2003
Johnson-McMillin syndrome, a neuroectodermal syndrome with conductive hearing loss and microtia: report of a new caseDaniela N Schweitzer, Shoji Yano, Dawn L Earl, et al.European Journal of Medical Genetics|April 1, 2009
A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosisMitchel J Pariani, Andrew Spencer, John M Graham, et al.Pageof 64