Kenneth W Dumars

Title(s)Professor Emeritus, Pediatrics
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(949) 644-5051
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    1. Association of terminal chromosome 1 deletion with sertoli cell-only syndrome. Am J Med Genet. 1998 Dec 04; 80(4):396-8. Hathout EH, Thompson K, Baum M, Dumars KW. PMID: 9856570.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    2. Practical guide to the diagnosis of thalassemia. Council of Regional Networks for Genetic Services (CORN). Am J Med Genet. 1996 Mar 01; 62(1):29-37. Dumars KW, Boehm C, Eckman JR, Giardina PJ, Lane PA, Shafer FE. PMID: 8779321.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    3. 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. J Biol Chem. 1989 Feb 15; 264(5):3002-6. Baldwin CT, Constantinou CD, Dumars KW, Prockop DJ. PMID: 2914942.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    4. Prevention of developmental disabilities: a model for organizing clinical activities. Res Dev Disabil. 1987; 8(4):507-20. Dumars KW, Gawron TW, Pearce CL, Foster CA. PMID: 2446356.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. The Southeast Asian refugee: the impact of cultural variation on the genetic counseling process. Birth Defects Orig Artic Ser. 1987; 23(6):239-44. Burney LR, Dumars KW, Chea CS, Nguyen HD, Bustillo AM. PMID: 3435766.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. Screening for developmental disabilities. West J Med. 1985 Sep; 143(3):349-56. Foster C, Duran-Flores D, Dumars KW, Stills S. PMID: 2413633.
      View in: PubMed   Mentions:    Fields:    Translation:HumansPHPublic Health
    7. Familial t(4;13) with abnormal offspring in three generations. Am J Med Genet. 1983 Sep; 16(1):15-22. Najafzadeh TM, Littman VA, Dumars KW. PMID: 6638065.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    8. Near-haploid cell line in the blastic crisis of chronic myelogenous leukemia: a possible marker for lymphoid malignancy. Cancer Genet Cytogenet. 1983 Aug; 9(4):333-9. Najafzadeh TM, Dumars GE, Dumars KW, Simpkins H, Katz J. PMID: 6603258.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    9. Amniotic-fluid-cell-culture failure and syringe toxicity revisited. Am J Hum Genet. 1982 Sep; 34(5):823-6. Ledbetter DH, Dumars KW, Carpenter RJ, Caskey CT. PMID: 7124736.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    10. Etiologic heterogeneity in hydranencephaly. Birth Defects Orig Artic Ser. 1982; 18(3B):229-35. Najafzadeh TM, Reinisch L, Dumars KW. PMID: 7139107.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    11. Antiviral activities of amniotic fluid. . 1981 Dec; 168(3):403-7. Cesario T, Goldstein A, Lindsey M, Dumars K, Tilles J. PMID: 6172794.
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    12. Three forms of dominant amyloid neuropathy. Johns Hopkins Med J. 1981 Dec; 149(6):239-47. Sack GH, Dumars KW, Gummerson KS, Law A, McKusick VA. PMID: 6975851.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    13. 9p duplication confirmed by gene dosage effect: report of two patients. Ann Genet. 1981; 24(4):242-4. Zadeh TM, Funderburk SJ, Carrel R, Dumars KW. PMID: 6977307.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    14. Duplication of distal 11q and 22p occurrence in two unrelated families. Am J Med Genet. 1981; 8(3):341-7. Najafzadeh TM, Dumars KW. PMID: 7234904.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    15. The dup(3q) syndrome: report of eight cases and review of the literature. Am J Med Genet. 1981; 10(2):159-77. Steinbach P, Adkins WN, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C. PMID: 7315873.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    16. Achalasia and microcephaly. Am J Med Genet. 1980; 6(4):309-14. Dumars KW, Williams JJ, Steele-Sandlin C. PMID: 7211947.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    17. The two faces of big brother. Hastings Cent Rep. 1979 Dec; 9(6):48. Dumars KW. PMID: 118946.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Genetic associate training program. J Med Educ. 1978 Sep; 53(9):768-70. Dumars KW. PMID: 691033.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    19. Minimizing the risk of amniocentesis for prenatal diagnosis. JAMA. 1977 Mar 28; 237(13):1336-8. Goldstein AI, Dumars KW. PMID: 402491.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCellsPHPublic Health
    20. Prenatal diagnosis of XYY karyotype. Am J Dis Child. 1976 Nov; 130(11):1295-6. Dumars KW, Fialko G, Willis J. PMID: 984014.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    21. Prenatal diagnosis and genetic counseling. West J Med. 1976 May; 124(5):377-87. Dumars KW, Dalrymple GT, Murray AK. PMID: 1274337.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    22. Prenatal diagnosis of chromosomal and enzymatic defects. Obstet Gynecol. 1976 Apr; 47(4):503-6. Goldstein A, Dumars KW, Kent DR. PMID: 130575.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    23. E trisomy phenotype associated with small metacentric chromosome and a familial Y-22 translocation. Birth Defects Orig Artic Ser. 1976; 12(5):97-104. Hanna RF, Ward TJ, Chow DS, Lagana SM, Moreira RK, Emond JC, Weintraub JL, Prince MR, Dumars KW, Fialko G, Larson E. PMID: 953249.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    24. X-autosome translocation with a 47,XXXY qs,t(9p-;Xq+) karyotype. Birth Defects Orig Artic Ser. 1975; 11(5):247-53. Dumars KW, Reed P, Lawce HJ. PMID: 1240775.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    25. Variation in pituitary-gonadal function in adolescent male homosexuals and heterosexuals. J Clin Endocrinol Metab. 1974 Oct; 39(4):796-801. Parks GA, Korth-Schütz S, Penny R, Hilding RF, Dumars KW, Frasier SD, New MI. PMID: 4416847.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    26. "True agonadism": a misnomer? J Pediatr. 1974 Mar; 84(3):375-80. Parks GA, Dumars KW, Limbeck GA, Quinlivan WL, New MI. PMID: 4272854.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    27. Cutis aplasia and cerebral malformation. Pediatrics. 1973 Dec; 52(6):861-4. Fowler GW, Dumars KW. PMID: 4129293.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    28. Fetal sex determination. Acta Cytol. 1973 May-Jun; 17(3):233-6. Adams C, Kilpatrick B, Kabacy G, Fialko G, Dumars KW. PMID: 4512462.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    29. Parental drug usage: effect upon chromosomes of progeny. Pediatrics. 1971 Jun; 47(6):1037-41. Dumars KW. PMID: 5141747.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    30. Median facial cleft associated with ring E chromosome. J Med Genet. 1970 Mar; 7(1):86-90. Dumars KW, Carnahan LG, Barrett RV. PMID: 5480971.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    31. Midline defects of the back: Pediatric view. GP. 1969 Oct; 40(4):132-7. Dumars KW. PMID: 4900499.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    32. Oculo-auriculo-vertebral dysplasia--Goldenhar's syndrome. Rocky Mt Med J. 1968 Apr; 65(4):44-6. Dumars K, Charles MA. PMID: 5646770.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    33. Gynecomastia, hypospermatogenesis and a large y chromosome in a man. Calif Med. 1968 Jan; 108(1):52-4. Dumars KW, Fisher CE. PMID: 18730098.
      View in: PubMed   Mentions: 1     Fields:    
    34. The adopted child and congenital malformations. Clin Pediatr (Phila). 1967 Dec; 6(12):696-8. Dumars KW. PMID: 6061351.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    35. Cancer, chromosomes and congenital abnormalities. Cancer. 1967 Jun; 20(6):1006-14. Dumars KW. PMID: 6067399.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    36. CHROMOSOME ANALYSIS--A LABORATORY SERVICE. Rocky Mt Med J. 1965 Jan; 62:37-41. DUMARS KW, GASKILL C . PMID: 14224481.
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    37. LE CRI DU CHAT (CRYING CAT) SYNDROME. Am J Dis Child. 1964 Nov; 108:533-7. DUMARS KW, GASKILL C, KITZMILLER N. PMID: 14209689.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    38. INCOMPLETE EXSTROPHY OF THE CLOACA. J Urol. 1964 May; 91:549-52. ROSENKRANTZ JG, BAILEY WC, DUMARS KW. PMID: 14154541.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    39. Effect of phenylalanine-restricted diet in phenylketonuria. II. AMA J Dis Child. 1957 Jun; 93(6):615-8. HORNER FA, STREAMER CW, CLADER DE, HASSELL LL, BINKLEY EL, DUMARS KW. PMID: 13424002.
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    40. Diphenhydramine (benadryl) and tripelennamine (pyribenzamine) intoxication in children. AMA Am J Dis Child. 1953 May; 85(5):545-50. JUDGE DJ, DUMARS KW. PMID: 13039563.
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    41. Potassium bromate poisoning. J Pediatr. 1949 Aug; 35(2):197-200. KITTO W, DUMARS KW. PMID: 18135538.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    42. Electro-shock therapy on patients complicated by skeletal pathology. Dis Nerv Syst. 1948 Oct; 9(10):300-4. GYSIN WM, DUMARS KW. PMID: 18889204.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
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