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JAMA|March 28, 1977
Minimizing the risk of amniocentesis for prenatal diagnosisA I Goldstein, K W DumarsAmerican Journal of Medical Genetics|January 1, 1981
Duplication of distal 11q and 22p occurrence in two unrelated familiesT M Najafzadeh, K W DumarsBirth Defects Original Article Series|January 1, 1976
E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocationK W Dumars, G Fialko, E LarsonBirth Defects Original Article Series|January 1, 1975
X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotypeK W Dumars, P Reed, H J LawceObstetrics and Gynecology|April 1, 1976
Prenatal diagnosis of chromosomal and enzymatic defectsA Goldstein, K W Dumars, D R KentThe Western Journal of Medicine|May 1, 1976
Prenatal diagnosis and genetic counselingK W Dumars, G T Dalrymple, A K MurrayAmerican Journal of Medical Genetics|January 1, 1980
Achalasia and microcephalyK W Dumars, J J Williams, C Steele-SandlinAmerican Journal of Medical Genetics|September 1, 1983
Familial t(4;13) with abnormal offspring in three generationsT M Najafzadeh, V A Littman, K W DumarsAmerican Journal of Medical Genetics|December 18, 1998
Association of terminal chromosome 1 deletion with sertoli cell-only syndromeE H Hathout, K Thompson, M Baum, et al.The Western Journal of Medicine|September 1, 1985
Screening for developmental disabilitiesC Foster, D Duran-Flores, K W Dumars, et al.Pageof 3