K. Dumars

发表

Practical guide to the diagnosis of thalassemia

C. Boehm, J. Eckman, P. Giardina, 1996 .

Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexuals.

R. Penny, M. New, K. Dumars, 1974, The Journal of clinical endocrinology and metabolism.

Effect of phenylalanine-restricted diet in phenylketonuria. II.

K. Dumars, F. Horner, C. W. Streamer, 1957, A.M.A. journal of diseases of children.

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 substitution near the carboxyl terminus destabilizes the whole triple helix.

C. Baldwin, D. Prockop, K. Dumars, 1989, The Journal of biological chemistry.

The dup(3q) syndrome: report of eight cases and review of the literature.

J. Opitz, L. Meisner, I. Hansmann, 1981, American journal of medical genetics.

Cutis aplasia and cerebral malformation.

K. Dumars, G. W. Fowler, 1973, Pediatrics.

Cancer, chromosomes and congenital abnormalities

N. Kitzmiller, K. Dumars, C. Gaskill, 1967, Cancer.

Antiviral Activities of Amniotic Fluid

T. Cesario, J. Tilles, K. Dumars, 1981, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Familial t(4;13) with abnormal offspring in three generations.

K. Dumars, T. M. Najafzadeh, V. Littman, 1983, American journal of medical genetics.

E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation.

K. Dumars, E. Larson, G. Fialko, 1976, Birth defects original article series.

X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype.

H. Lawce, K. Dumars, P. Reed, 1975, Birth defects original article series.

"True agonadism": a misnomer?

M. New, K. Dumars, G. A. Limbeck, 1974, The Journal of pediatrics.

LE CRI DU CHAT (CRYING CAT) SYNDROME.

N. Kitzmiller, K. Dumars, C. Gaskill, 1964, American journal of diseases of children.

INCOMPLETE EXSTROPHY OF THE CLOACA.

K. Dumars, J. Rosenkrantz, W. C. Bailey, 1964, The Journal of urology.

Fetal sex determination.

K. Dumars, B. Kilpatrick, G. Kabacy, 1973, Acta cytologica.

Diphenhydramine (benadryl) and tripelennamine (pyribenzamine) intoxication in children.

K. Dumars, D. Judge, 1953, A.M.A. American journal of diseases of children.

Electro-shock therapy on patients complicated by skeletal pathology.

K. Dumars, W. Gysin, 1948, Diseases of the nervous system.

Median facial cleft associated with ring E chromosome.

R. Barrett, K. Dumars, L. G. Carnahan, 1970, Journal of medical genetics.

Three forms of dominant amyloid neuropathy.

V. McKusick, G. Sack, K. Dumars, 1981, The Johns Hopkins medical journal.

9p duplication confirmed by gene dosage effect: report of two patients.

K. Dumars, R. Carrel, S. Funderburk, 1981, Annales de genetique.

Amniotic-fluid-cell-culture failure and syringe toxicity revisited.

D. Ledbetter, C. Caskey, R. Carpenter, 1982, American journal of human genetics.

Near-haploid cell line in the blastic crisis of chronic myelogenous leukemia: a possible marker for lymphoid malignancy.

K. Dumars, H. Simpkins, J. Katz, 1983, Cancer genetics and cytogenetics.

Duplication of distal 11q and 22p occurrence in two unrelated families.

K. Dumars, T. M. Najafzadeh, 1981, American journal of medical genetics.

Practical guide to the diagnosis of thalassemia. Council of Regional Networks for Genetic Services (CORN).

C. Boehm, J. Eckman, P. Giardina, 1996, American journal of medical genetics.

Potassium bromate poisoning.

K. Dumars, W. Kitto, 1949, The Journal of pediatrics.

PEDIATRIC EPILEPTOLOGY—CLASSIFICATION AND MANAGEMENT OF SEIZURES IN CHILDREN

K. Dumars, 1985 .

Prenatal diagnosis of XYY karyotype.

J. Willis, K. Dumars, G. Fialko, 1976, American journal of diseases of children.

Prenatal detection of chromosomal mosaicism

K. Dumars, T. M. Najafzadeh, T. Cahill, 1982 .

Achalasia and microcephaly.

K. Dumars, J. Williams, C. Steele-Sandlin, 1980, American journal of medical genetics.