Pierre Robin Sequence Associated With First Trimester Fetal Tamoxifen ExposureBERGER, Joel C; CLERICUZIO, Carol L.American journal of medical genetics. Part A. 2008, Vol 146, Num 16, pp 2141-2144, issn 1552-4825, 4 p.Article

Hydranencephaly in an infant with vascular malformationsSTEVENSON, David A; HART, Blaine L; CLERICUZIO, Carol L et al.American journal of medical genetics. 2001, Vol 104, Num 4, pp 295-298, issn 0148-7299Article

Emotion-related learning in individuals prenatally exposed to alcohol: an investigation of the relation between set shifting, extinction of responses, and behaviorKODITUWAKKU, Piyadasa W; MAY, Philip A; CLERICUZIO, Carol L et al.Neuropsychologia. 2001, Vol 39, Num 7, pp 699-708, issn 0028-3932Article

Deletions and Duplications of Developmental Pathway Genes in 5q31 Contribute to Abnormal PhenotypesROSENFELD, Jill A; MILISA DRAUTZ, Joanne; LAMB, Allen N et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 8, pp 1906-1916, issn 1552-4825, 11 p.Article

Unexpected death and critical illness in Prader-Willi syndrome: Report of ten individualsSTEVENSON, David A; ANAYA, Theresa M; CLAYTON-SMITH, Jill et al.American journal of medical genetics. 2004, Vol 124A, Num 2, pp 158-164, issn 0148-7299, 7 p.Article

Two New Patients With Curry-Jones Syndrome With Trichoblastoma and Medulloblastoma Suggest an Etiologic Role of the Sonic Hedgehog-Patched-GLI PathwayGRANGE, Dorothy K; CLERICUZIO, Carol L; BAYLISS, Susan J et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 20, pp 2589-2597, issn 1552-4825, 9 p.Article

Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patientsWANG, Lisa L; GANNAVARAPU, Anu; CLERICUZIO, Carol L et al.American journal of medical genetics. 2003, Vol 118A, Num 3, pp 299-301, issn 0148-7299, 3 p.Article

Deaths due to choking in Prader-Willi syndromeSTEVENSON, David A; HEINEMANN, Janalee; ANGULO, Moris et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 5, pp 484-487, issn 1552-4825, 4 p.Article

Risk for leukemia in infants without down syndrome who have transient myeloproliferative disorderGUSHING, Thomas; CLERICUZIO, Carol L; WILSON, Carla S et al.The Journal of pediatrics. 2006, Vol 148, Num 5, pp 687-689, issn 0022-3476, 3 p.Article

A New Hypothesis of OCA1BCHIANG, Pei-Wen; DRAUTZ, Joanne M; TSAI, Anne Chun-Hui et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 22, pp 2968-2970, issn 1552-4825, 3 p.Article

Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasiaCLERICUZIO, Carol L; CHEN, Emily; MCNEIL, Dawn Elizabeth et al.The Journal of pediatrics. 2003, Vol 143, Num 2, pp 270-272, issn 0022-3476, 3 p.Article

Limb Hyperplasia: Case Report of an Unusual Variant of Klippel-Trenaunay Syndrome and Review of the LiteratureGOBER-WILCOX, Julie K; GARDNER, David L; JOSTE, Nancy E et al.Cutis (New York, NY). 2009, Vol 83, Num 5, pp 255-262, issn 0011-4162, 8 p.Article

A New Syndrome With Multiple Capillary Malformations, Intractable Seizures, and Brain and Limb AnomaliesCARTER, Melissa T; GERAGHTY, Michael T; DE LA CRUZ, Laura et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 301-306, issn 1552-4825, 6 p.Article

Diagnosing Xeroderma Pigmentosum Group C by ImmunohistochemistryDE FERAUDY, Sébastien; BOUBAKOUR-AZZOUZ, Imenne; FRAITAG, Sylvie et al.The American journal of dermatopathology. 2010, Vol 32, Num 2, pp 109-117, issn 0193-1091, 9 p.Article

Neuroimaging Findings in Macrocephaly-Capillary Malformation : A Longitudinal Study of 17 PatientsCONWAY, Robert L; PRESSMAN, Barry D; CLERICUZIO, Carol L et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 24, pp 2981-3008, issn 1552-4825, 28 p.Article

Marshall-Smith syndrome : Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalitiesADAM, Margaret P; HENNEKAM, Raoul C. M; KEPPEN, Laura Davis et al.American journal of medical genetics. 2005, Vol 137A, Num 2, pp 117-124, issn 0148-7299, 8 p.Article

Athabascan brainstem dysgenesis syndromeHOLVE, Steve; FRIEDMAN, Barbara; HOYME, H. Eugene et al.American journal of medical genetics. 2003, Vol 120A, Num 2, pp 169-173, issn 0148-7299, 5 p.Article