Natural history of Williams syndrome: Physical characteristics von Morris, Colleen A., Demsey, Susan A., Leonard, Claire O., Dilts, Constance, Blackburn, Brent L.

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Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2 von Robin, Nathaniel H, Feldman, George J, Aronson, Adam L, Mitchell, Heather F, Weksberg, Rosanna, Leonard, Claire O, Burton, Barbara K, Josephson, Kevin D, Laxová, Renata, Aleck, Kyrieckos A, Allanson, Judith E, Guion-Almeida, Maria Leine, Martin, Rick A, Leichtman, Lawrence G, Price, R. Arlen, Opitz, John M, Muenke, Maximilian

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Strong correlation of elastin deletions, detected by FISH, with Williams syndrome : evaluation of 235 patients von LOWERY, M. C, MORRIS, C. A, EWART, A, BROTHMAN, L. J, XIAO LIN ZHU, LEONARD, C. O, CAREY, J. C, KEATING, M, BROTHMAN, A. R

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Children and adolescents with neurofibromatosis 1 : A behavioral phenotype von DILTS, C. V, CAREY, J. C, KIRCHER, J. C, HOFFMAN, R. O, CREEL, D, WARD, K, CLARK, E, LEONARD, C. O

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SERUM AFP SCREENING FOR NEURAL TUBE DEFECTS von LEONARD, CLAIRE O

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Bone mineral status in children with phenylketonuria— relationship to nutritional intake and phenylalanine control von McMurry, MP, Chan, GM, Leonard, CO, Ernst, SL

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Genetic counseling von Leonard, Claire O, Chase, G A, Childs, Barton

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Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cells von Kaback, M M, Leonard, C O, Parmley, T H

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Opitz (BBB/G) syndrome: Oral manifestations von Brooks, John K., Leonard, Claire O., Coccaro Jr, Peter J.

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Issues in newborn screening. (American Academy of Pediatrics) von McCabe, Edward R.B, Leonard, Claire O, Medici, Frank N, Seashore, Margretta R, Weiss, Lester, de la Cruz, Felix, Elias, Sherman, Lin-Fu, Jane, Oakley, Godfrey

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Testing for inborn errors of metabolism in the acutely ill newborn von LEONARD, C. O, NUTTALL, K. L

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Prenatal screening and pregnant women's attitudes toward the abortion of defective fetuses von Faden, R R, Chwalow, A J, Quaid, K, Chase, G A, Lopes, C, Leonard, C O, Holtzman, N A

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Respiratory complications of achondroplasia von Stokes, Dennis C., Phillips, John A., Leonard, Claire O., Dorst, John P., Kopits, Steven E., Trojak, Joseph E., Brown, David L.

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Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: The M syndrome von Rauch, Anita, Feindt, Karla A., Leonard, Claire O., Thompson, Joel A., Hoffman, Robert O., Creel, Donnell J., Opitz, John M.

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Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiency von Spence, J. Edward, Maddalena, Anne, O'Brien, William E., Fernbach, Susan D., Batshaw, Mark L., Leonard, Claire O., Beaudet, Arthur L.

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What participants understand about a maternal serum alpha-fetoprotein screening program von Faden, R R, Chwalow, A J, Orel-Crosby, E, Holtzman, N A, Chase, G A, Leonard, C O

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Maternal Phenylketonuria von McCabe, Edward R.B, Leonard, Claire O, Medici, Frank N, Seashore, Margretta R, Weiss, Lester, Cruz, Felix de la, Elias, Sherman, Lin-Fu, Jane, Oakley, Godfrey

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Maternal serum alpha-fetoprotein screening. (American Academy of Pediatrics Committee on Genetics guidelines) von McCabe, Edward R.B, Leonard, Claire O, Medici, Frank N, Seashore, Margretta R, Weiss, Lester, Cruz, Felix de la, Elias, Sherman, Lin-Fu, Jane, Oakley, Godfrey

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PRENATAL DIAGNOSIS OF FACTOR VIII DEFICIENCY TO HELP WITH THE MANAGEMENT OF PREGNANCY AND DELIVERY von Baty, BonnieJeanne, Drayna, Dennis, Leonard, ClaireO, White, Ray

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Spina bifida: a new disease von Leonard, C O, Freeman, J M

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