A single base mutation that converts glycine 907 of the alpha 2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta. The single amino acid su... von Baldwin, C T, Constantinou, C D, Dumars, K W, Prockop, D J

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Parental drug usage: effect upon chromosomes of progeny von Dumars, Jr, K W

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The Adopted Child and Congenital Malformations von Dumars, K.W.

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Genetic associate training program von Dumars, K W

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Cancer, chromosomes and congenital abnormalities von Dumars, K. W., Kitzmiller, Nancy, Gaskill, Catherine

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A single base mutation that converts glycine 907 of the α2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta: the single amino acid substit... von BALDWIN, C. T, CONSTANTINOU, C. D, DUMARS, K. W, PROCKOP, D. J

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Prevention of developmental disabilities: A model for organizing clinical activities von Dumars, Kenneth W., Gawron, Timothy W., Pearce, Catherine L., Foster, Carol A.

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Amniotic-fluid-cell-culture failure and syringe toxicity revisited von Ledbetter, D H, Dumars, K W, Carpenter, R J, Caskey, C T

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Screening for Developmental Disabilities von Foster, Carol, Duran-Flores, Deborah, Dumars, Kenneth W., Stills, Stanley

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Cutis aplasia and cerebral malformation von Fowler, G W, Dumars, K W

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PRENATAL DIAGNOSIS OF CHROMOSOMAL AND ENZYMATIC DEFECTS von Goldstein, Arthur, Dumars, Kenneth W., Kent, Deryck R.

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Familial t(4;13) with abnormal offspring in three generations von Najafzadeh, Touran M., Littman, Vicki A., Dumars, Kenneth W., Opitz, John M.

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Prenatal Diagnosis and Genetic Counseling von Dumars, Kenneth W., Dalrymple, Gisela T., Murray, Allen K.

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Gynecomastia, hypospermatogenesis and a large y chromosome in a man von Dumars, K W, Fisher, C E

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Achalasia and microcephaly von Dumars, Kenneth W., Williams, James J., Steele-Sandlin, Constance, Holmes, Lewis B.

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Association of terminal chromosome 1 deletion with Sertoli cell-only syndrome von Hathout, Eba H., Thompson, Kevin, Baum, Marti, Dumars, Kenneth W.

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Median facial cleft associated with ring E chromosome von Dumars, K W, Carnahan, L G, Barrett, R V

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Practical guide to the diagnosis of thalassemia von Dumars, Kenneth W., Boehm, Corinne, Eckman, James R., Giardina, Patricia J., Lane, Peter A., Shafer, Frank E.

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Duplication of distal 11q and 22p occurrence in two unrelated families von Najafzadeh, Touran M., Dumars, Kenneth W., Opitz, John M.

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“True agonadism”: A misnomer? von Parks, Gary A., Dumars, Kenneth W., Limbeck, George A., Quinlivan, W. Leslie, New, Maria I.

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