Portal de Periódicos da CAPES

In memoriam. Dr. Peter Browen, 1932–1988

1990; Wiley; Volume: 35; Issue: 1 Linguagem: Inglês

10.1002/ajmg.1320350126

1096-8628

Patrick Ferreira,

Sexual Differentiation and Disorders

American Journal of Medical GeneticsVolume 35, Issue 1 p. 136-138 Obituary In memoriam. Dr. Peter Browen, 1932–1988 Patrick Ferreira, Corresponding Author Patrick Ferreira Division of Medical Genetics, Department of Pediatrics, University of Alberta, Edmonton, Alberta, CanadaDivision of Medical Genetics, Dept. of Pediatrics, University of Alberta, Clinical Sciences Bldg. 4-117, 8440-112 Street, Edmonton, Alberta T6G 2B7 CanadaSearch for more papers by this author Patrick Ferreira, Corresponding Author Patrick Ferreira Division of Medical Genetics, Department of Pediatrics, University of Alberta, Edmonton, Alberta, CanadaDivision of Medical Genetics, Dept. of Pediatrics, University of Alberta, Clinical Sciences Bldg. 4-117, 8440-112 Street, Edmonton, Alberta T6G 2B7 CanadaSearch for more papers by this author First published: January 1990 https://doi.org/10.1002/ajmg.1320350126Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References Bowen P (1985): Invited editorial comment: Workshop on genetic disorders in the Hutterites-Edmonton, Canada, October 12-13, 1983. Am J Med Genet 22: 449–451. Bowen P, Biederman B, Hoo JJ (1985): The critical segment for the Langer-Giedion syndrome: 8q24.11 - q11.21 in cat-eye syndrome. Am J Med Genet 24: 543–545, (1986). Lin CC, Bowen P, Hoo JJ: Familial paracentric inversions inv(2) (q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities. Hum Genet 75: 84–87, (1987). Samuel IP, Bowen P, Lin CC, Hoo JJ: Prenatal diagnosis and the Prader-Willi syndrome. Karyogram 14: 88–90, (1988). Canadian Collaborative CVS Amniocentesis clinical trial Group–Olley P, Bowen P, Tataryn I, Choi M, Reid D, Pyatt Z, et al.: Multicentre randomised clinical trial of chorion villus sampling and amniocentesis: first report. Lancet 1: 1–6, (1989). Varnhagen CK, Lewin S, Das JP, Bowen P, Ma K, Klimek M: Neurofibromatosis and Psychological Processes. J Dev Behav Pediatr 9: 257–265, (1988). Lowry RB, Bowen P: The Alberta Hereditary Disease Program: A regional model for delivery of genetic services. Submitted to CMAJ, (1989). Bowen P: An unusual cardiomelic syndrome. Letter to the editor. Submitted to Am J Med Genet, (1989). Lin CC, Sasi R, Bowen P, Unger T, Tainaka T: Identification of Y-specific DNA sequences in a Turner Syndrome with 45, X/45, X, +marker chromosome mosaicism and normal stature. In preparation, (1988). Slater JD, Yanofsky M, Bowen P, Lin CC: 47, XXY Karyotype in lymphoblasts in congenital leukemia. In preparation, (1988). Bowen P, Sisson W, Berner M, Harris H, Hopkinson DA: Pepsinogen polymorphism: evidence for a third common allele. Clin Res 20: 929, (1972). Bowen P: Studies of pepsinogen isozymes in urine and gastric mucosa. Abstract 16A, 26th American Society of Human Genetics, Portland ( 1974). Bowen P: Developmental patterns of proteolytic isoenzymes in stomach and duodenum and observations on a fetal pepsinogen. Clin Res 22: 5, 735A, (1974). Biederman B, Bowen P, Swallow K: Mental retardation with macroorchidism and pedigree consistent with X-linked inheritance. (1976) Birth Defects Conference, National Foundation March of Dimes. University of British Columbia, Vancouver, BC. Bowen P, Biederman B, Gauk E, Von Koenigsloew E: Familial r(21) chromosome with distal deletion and trisomy for a proximal segment of chromosome 21 in different members. Fifth International Congress of Human Genetics, Mexico, DF, Excerpta Medica (1976). Biederman B, Bowen P: De novo partial monosomy 7Q in a patient with a familial balanced translocation. 46, XX, del(7)(q33), t(8:9)(q11:q31)pat. (1977) Birth Defects Conference, National Foundation March of Dimes, University of Tennessee Center for the National Sciences, Memphis, Tennessee. Bowen P, Lentle BC, Jackson FI, Percy JS, Rigal WM: Abnormal localization of 67-Gallium citrate in dystrophic muscle. Clin Res 26: 175A, (1978). Schurig V, Bowen P, Harley F, Schiff D: The Meckel syndrome in the Hutterites: variable expression and long survival. (1979) Birth Defects Conference, National Foundation March of Dimes, Northwestern Medical School, Chicago, Illinois. Schurig V, Van Orman A, Bowen P: Genetic disorders in the Hutterites. (1980) Birth Defects Conference, National Foundation March of Dimes, New York, New York. Lin CC, Bowen P, De Braekeleer M: Paracentric inversion in the long arms of chromosome 2 and 8 associated with recurrent abortions and Giedion-Langer syndrome respectively Abstract C 1.75 7th International congress Human Genetics Berlin(west) (1986). Appendix A: Publications Bowen P, Lee CSN: Ph1 chromosome in the diagnosis of chronic myeloid leukemia: report of case with features simulating myelofibrosis. Bull Johns Hopkins Hosp 113: 1–12, July 1963. Lindsten J, Bowen P, Lee CSN, McKusick VA, Polani PE, Wingate M, Edwards JH, Hamper J, Tippett P, Sanger R, Race RR: Source of the X in XO females: The evidence of Xg. Lancet i: 558–559, 1963. Bowen P, Lee CSN, Zellweger H, et al.: A familial syndrome of multiple congenital defects. Bull Johns Hopkins Hosp 144: 402–414, June 1964. Lee CSN, Bown P, Rosenblum H, et al.: Familial chromosome -2,3 translocation ascertained through an infant with multiple malformations. N Engl J Medd 271: 12–16, July 1964. Ferguson-Smith M, Alexander DS, Bown P, et al.: Clinical and cytogenetical studies in female gonadal dysgenesis and their bearing on the cause of Turner's syndrome. Cytogenetics (Base 1) 3: 355–383, 1964. Bowen P: Chromosomal abnormalities. Clin Orthop 33: 40–58, March-April 1964. Bowen P, Lee CSN, Migeon CJ, Kaplan NM, Whalley PJ, McKusick VA, Reifenstein EC, Jr.: Hereditary male pseudohermaphroditism with hypogonadism, hypospadias, and gynecomastia (Reifenstein's syndrome). Ann Intern Med 62: 252–270, 1965. Bowen P, Ferguson-Smith MA, Mosier D, et al.: The Laurence-Moon syndrome association with hypogonadotrophic, hypogonadism and sex-chromosome aneuploidy. Arch Intern Med (Chicago) 116: 596–604, October 1965. Lee CSN, Boyer SH, Bowen P, et al.: The D1 trisomy syndrome: Three subjects with unequally advancing development. Bull Johns Hopkins Hosp 118: 374–394, May 1966. Bowen P, Lee CSN, Harvey JC, et al.: Comparison of non-modal chromosome counts in individuals affected with myotonic dystrophy and in control subjects. Am J Med Sci 255: 358–367, June 1968. Bowen P, Lee CSN, Harvey JC: Balanced reciprocal translocation between two D-group chromosomes in a family with myotonic dystrophy. Am J Med Sci 255: 368–375, June 1968. Nicholson SF, Thurston OG, Bowen P: Chromosomes of the Walker 256 rat mammary carcinoma: Observations on primary and metastatic tumors of a new subline with a pseudodiploid karyotype. J Natl Cancer Inst 41: 217–227, 1968. Bowen P, Lee CS: Spontaneous abortion. Chromosome studies on 41 cases and analysis of maternal age and duration of pregnancy in relation to karyotype. Am J Obstet Gynecol 104: 973–983, August 1969. Bowen P, Lee CSN, Shea DR: Polydactyly and other minor stigmata associated with 46,XX/47,XX, D + mosaicism. Can Med Assoc J 102: 49–51, January 1970. Bowen P, O'Callaghan F, Lee CS: Serum protein polymorphisms in Indians in western Canada. Hum Hered 21: 242–253, 1971. Bowen P, Armstrong HB: Cleft lip-palate, ectodermal dysplasia, handfoot anomalies and oligophrenia. Birth Defects Atlas and compendium, p 262, 1973. Lee CSN, Ping KL, Bowen P: Position of the Duffy locus on chromosome 1 in relation to break points for structural rearrangements. Am J Hum Genet 26: 93–102, January 1974. Bowen P: Achondroplasia in two sisters with normal parents. Birth Defects 10(10): 31–36, 1974. Bowen P, Chernick BC, Campbell DJ, et al.: Mild characteristics of Down syndrome with normal karyotype in cultured lymphocytes and skin fibroblasts. Birth Defects 10(10): 83–8, 1974. Bowen P, Ying KL, Chung GH: Trisomy 9 mosaicism in a newborn infant with multiple malformations. J Pediatr 85: 95–7, July 1974. Bowen P, Harley F: Mandibulofacial dysostosis with limb malformations (Nager's acrofacial dysostosis). Birth Defects 10(5): 109–15, 1974. Bowen P, Armstrong HB: Ectodermal dysplasia, mental retardation, cleft lip/palate and other anomalies in three sibs. Clin Genet 9: 35–42, January 1976. Biederman B, Bowen P: Partial trisomy 4q due to familial 2/4 translocation. Hum Genet 33(2): 147–53, 1976. Bowen P, Conradi GJ: Syndrome of skeletal and genitourinary anomalies with unusual facies and failure to thrive in Hutterite sibs. Birth Defects 12(6): 101–108, 1976. Biederman B, Bowen P: Balanced translocation involving chromosome 12: report of a case and possible evidence for a position effect. Ann Genet (Paris) 19(4): 257–60, December 1976. Biederman B, Bowen P, Aronson MM, et al.: A (2:4) translocation, unbalanced, 46 chromosomes. Repository identification No. GM-501. Cytogenet Cell Genet 17: 298–299, 1976. Biederman B, Bozuen P, Aronson MM, et al.: A (2;4) translocation, balanced, 46 chromosomes: Repository Identification NO. GM-1064. Cytogenet Cell Genet 17(5): 300–01, 1976. Lewis M, Kaita H, Chown B, Bowen P, Lee CSN, et al.: A genetic linkage analysis of chromosome 6 markers Chido, HLA and glyoxalase. Birth Defects 12(7): 317–321, 1976. Biederman B, Bowen P, Robertson D, et al.: Partial trisomy 12p due to t(12;Zl)pat translocation. Hum Genet 36: 35–41, April 1977. Bowen P, Lentle BC, Jackson FI, Percy JS, Riga1 WM: Abnormal localisation of gallium-67 citrate in pseudohypertrophic muscular dystrophy. Lancet 2: 1072–1073, 1977. Jugdutt BJ, Duncan NF, Bowen P, et al.: The Marfan syndrome, coarctation of the aorta and precocious puberty. Chest 71(6): 797–798, June 1977. Lin CC, Holman G, Sewell L, Bowen P, Biederman B: Interchromosomal duplication for the short arm of chromosome 9: report of three cases due to a familial translocation t(9:II) and one case with a de novo 47,XX, +9p karyotype. J Ment Defic Res 21: 309–329, 1977. Biederman B, Bowen P, Swallow KA: Mental retardation with macroorchidism and pedigree consistent with X-linked inheritance. Birth Defects 13(3C), 224–225, 1977. Bowen P: Genetics factos in mental retardation. Mental Retardation for Special Educators 3–30. JP Das and D Baine (eds). Charles C. Thomas, Springfield, IL, 1978. Jackson FI, Bowen P, Lentle BC: Scintilymphangiography with 99m Tc antimony sulfide colloid in hereditary lymphedema (Nonne-Milroy disease). Clin Nucl Med 3: 296–98, 1978. Finer NN, Bowen P, Dunbar LG: Caudal regression anomalad (sacral agenesis) in siblings. Clin Genet 13: 353–58, 1978. Biederman B, Bowen P: Balanced t(8:9)(q12:q33)pat carrier with phenolypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7. Hum Genet 41: 101–07, 1978. Bowen P, Biederman B, Swallowv KA: The X-linked syndrome of macroorchidism and mental retardation: further observations. Am J Med Genet 2: 409–14, 1978. Schurig V, Bowen P, Harley F, Schiff D: The Meckel syndrome in Hutterites. Am J Med Genet 5: 373–82, 1980. Schurig V, Van Orman A, Bowen P: Nonprogressive cerebellar disorder with mental retardation and autosomal recessive heritance in Hutterites. Am J Med Genet 9: 43–53, 1981. Bowen P, Lowry RB: Genetic disorders in Hutterites. Bulletin of the Hereditary Diseases Program of Alberta. 1: 9–10, 1982. Herbert FA, Bowen P: Hereditary late-onset lymphedema with pleural effusion and laryngeal edema. Arch Intern Med 143: 913–915, 1983. Bowen P, Fitzgerald PH, Gardner RJM, Biederman B, Veale AMO: Duplication 8q syndrome due to familial chromosome ins(10:8) (q21:q212q22). Am J Med Genet 14: 635–646, 1983. Toth EL, Rowen PA, Crockford PM: Hereditary central diabetes insipidus: plasma levels of antidiuretic hormone in a family with a possible osmoreceptor defect. Can Med Assoc J 131: 1237–1241, 1984. Bowen P: Workshop on genetic disorders in the Hutterites-Edmonton, Canada October 12–13. Invited editorial comment. Am J Med Genet 22: 449–451, 1985. Gibson KM, Sweetman L, Nyhan WL, Bowen P: Clinical correlation of dysequilibrium syndrome and 4-Hydroxybutyric aciduria. J Inher Metab Dis 8: 58, 1985. Bowen P, Biederman B, Hoo JJ: The critical segment for the Langer-Giedion syndrome: 8q24.11- q11.21 in cat-eye syndrome. Am J Med Genet 24: 543–545, 1986. Lin CC, Bowen P, Hoo JJ: Familial paracentric inversions inv(2) (q31q35) and inv(8)(q22.3q24.13) ascertained through reproductive abnormalities. Hum Genet 75: 84–87, 1987. Samuel IP, Bowen P, Lin CC, Hoo JJ: Prenatal diagnosis and the Prader-Willi syndrome. Karyogram 14: 88–90, 1988. Canadian Collaborative CVS Amniocentesis clinical trial Group Olley P. Bowen P, Tataryn I, Choi M, Reid D, Pyatt Z, et al.: Multicentre randomised clinical trial of chorion villus sampling and amniocentesis: first report. Lancet 1: 1–6, 1989. Varnhagen CK, Lewin S, Das JP, Bowen P, Ma K, Klimek M: Neurofibromatosis and Psychological Processes. J Dev Behav Pediatr 9: 257–265, 1988. Lowry RB, Bowen P: The Alberta Hereditary Disease Program: A regional model for delivery of genetic services. Submitted to CMAJ, 1989. Bowen P: An unusual cardiomelic syndrome. Letter to the editor. Submitted to Am J Med Genet, 1989. Lin CC, Sasi R, Bowen P, Unger T, Tainaka T: Identification of Y-specific DNA sequences in a Turner Syndrome with 45,X/45,X, +marker chromosome mosaicism and normal stature. In preparation, 1988. Slater JD, Yanofsky M, Bowen P, Lin CC: 47,XXY Karyotype in lymphoblasts in congenital leukemia. In preparation, 1988. Appendix B: Abstracts Bowen P, Sisson W, Berner M, Harris H, Hopkinson DA: Pepsinogen polymorphism: evidence for a third common allele. Clin Res 20: 929, 1972. Bowen P: Studies of pepsinogen isozymes in urine and gastric mucosa. Abstract 16A, 26th American Society of Human Genetics, Portland 1974. Bowen P: Developmental patterns of proteolytic isoenzymes in stomach and duodenum and observations on a fetal pepsinogen. Clin Res 22:5, 135A, 1974. Biederman B, Bowen P, Swallow K: Mental retardation with macroorchidism and pedigree consistent with X-linked inheritance. 1976 Birth Defects Conference, National Foundation March of Dimes. University of British Columbia, Vancouver, BC. Bowen P, Biederman B, Gauk E, Von Koenigsloew E: Familial r(21) chromosome with distal deletion and trisomy for a proximal segment of chromosome 21 in different members. Fifth International Congress of Human Genetics, Mexico, DF, Excerpta Medica 1976. Biederman B, Bowen P: De novo partial monosomy 7Q in a patient with a familial balanced translocation. 46,XX, de1(7)(q33), t(8:9)(qll:q31)pat. 1977 Birth Defects Conference, National Foundation March of Dimes, University of Tennessee Center for the National Sciences, Memphis, Tennessee. Bowen P, Lentle BC, Jackson FI, Percy JS, Rigal WM: Abnormal localization of 67-Gallium citrate in dystrophic muscle. Clin Res 26: 175A, 1978. Schurig V, Bowen P, Harley F, Schiff D: The Meckel syndrome in the Hutterites: variable expression and long survival. 1979 Birth Defects conference, National Foundation March of Dimes, Northwestern Medical School, Chicago, Illinois. Schurig V, Van Orman A, Bowen P: Genetic disorders in the Hutterites. 1980 Birth Defects Conference, National Foundation March of Dimes, New York, New York. Lin CC, Bowen P, De Braekeleer M: Paracentric inversion in the long arms of chromosome 2 and 8 associated with recurrent abortions and Giedion-Langer syndrome respectively Abstract C 1.75 7th International congress Human Genetics Berlin(west) 1986. Volume35, Issue1January 1990Pages 136-138 ReferencesRelatedInformation