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Growth spurt hypocalcemiaWRIGHT, Kathryn L; BAWLE, Erawati V.Journal of adolescent health. 2006, Vol 38, Num 6, pp 772-775, issn 1054-139X, 4 p.Article

Arginine deficiency-induced hyperammonemia in a home total parenteral nutrition-dependent patient: A case reportKAPILA, Shikha; SABA, May; LIN, Chuan-Hao et al.JPEN. Journal of parenteral and enteral nutrition. 2001, Vol 25, Num 5, pp 286-288, issn 0148-6071Article

Picture of the monthKADDU, Rajiv; BAWLE, Erawati V; TOLIA, Vasundhara et al.Archives of pediatrics & adolescent medicine. 2001, Vol 155, Num 1, pp 87-88, issn 1072-4710Article

Transmission of ring chromosome 13 from a mother to daughter with both having a 46,XX, r(13)(p13q34) karyotypeBEDOYAN, Jirair K; FLORE, Leigh Anne; ALKATIB, Aziz et al.American journal of medical genetics. 2004, Vol 129A, Num 3, pp 316-320, issn 0148-7299, 5 p.Article

The neuropsychological phenotype of velocardiofacial syndrome (VCFS) : Relationship to psychopathologyLAJINESS-O'NEILL, Renée; BEAULIEU, Isabelle; ASAMOAH, Alexander et al.Archives of clinical neuropsychology. 2006, Vol 21, Num 2, pp 175-184, issn 0887-6177, 10 p.Article

Medulloblastoma with adverse reaction to radiation therapy in Nijmegen breakage syndromeBAKHSHI, Sameer; CEROSALETTI, Karen M; CONCANNON, Patrick et al.Journal of pediatric hematology/oncology. 2003, Vol 25, Num 3, pp 248-251, issn 1077-4114, 4 p.Article

A syndrome of hypoplastic sinuses, hydrocephalus, bronchiectasis, and hypogammaglobulinemia with functional antibody deficiency in twin girlsBARBIERI, Elaine A; BAWLE, Erawati B; TODER, Debbie S et al.Annals of allergy, asthma, & immunology. 2005, Vol 94, Num 6, pp 693-699, issn 1081-1206, 7 p.Article

Duplication of the STS Region in Males Is a Benign Copy-Number VariantFURROW, Aubry; THEISEN, Aaron; VELSHER, Lea et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 8, pp 1972-1975, issn 1552-4825, 4 p.Article

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndromeDUKER, Angela L; BALLIF, Blake C; ROSENFELD, Jill A et al.European journal of human genetics. 2010, Vol 18, Num 11, pp 1196-1201, issn 1018-4813, 6 p.Article

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