Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients - PubMed (original) (raw)
. 1969 Mar;21(2):196-227.
- PMID: 5770175
- PMCID: PMC1706430
Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients
J German. Am J Hum Genet. 1969 Mar.
No abstract available
Similar articles
- [Bloom's syndrome].
Kirchner M, Hesse V. Kirchner M, et al. Humangenetik. 1972;15(1):25-32. doi: 10.1007/BF00273428. Humangenetik. 1972. PMID: 5046905 German. No abstract available. - [Intra-uterine nanism with telangiectasic erythema and chromosome anomalies: Bloom's syndrome].
Sizonenko P, Job JC, Kreisler L, Rossier A. Sizonenko P, et al. Ann Pediatr (Paris). 1967 Oct 2;14(10):2404-8. Ann Pediatr (Paris). 1967. PMID: 5621830 French. No abstract available. - [Spontaneous chromosomal instability in the rare hereditary diseases: Fanconi's anemia and Bloom's syndrome].
Schroeder TM. Schroeder TM. Dtsch Med Wochenschr. 1973 Nov 16;98(46):2213-5. doi: 10.1055/s-0028-1107226. Dtsch Med Wochenschr. 1973. PMID: 4757391 German. No abstract available. - Genes which increase chromosomal instability in somatic cells and predispose to cancer.
German J. German J. Prog Med Genet. 1972;8:61-101. Prog Med Genet. 1972. PMID: 4557110 Review. No abstract available. - [Heredity in leukemia].
Kurita S. Kurita S. Nihon Rinsho. 1971;29(6):1494-502. Nihon Rinsho. 1971. PMID: 4253936 Review. Japanese. No abstract available.
Cited by
- The BLM helicase is a new therapeutic target in multiple myeloma involved in replication stress survival and drug resistance.
Ovejero S, Viziteu E, Dutrieux L, Devin J, Lin YL, Alaterre E, Jourdan M, Basbous J, Requirand G, Robert N, de Boussac H, Seckinger A, Hose D, Vincent L, Herbaux C, Constantinou A, Pasero P, Moreaux J. Ovejero S, et al. Front Immunol. 2022 Dec 9;13:983181. doi: 10.3389/fimmu.2022.983181. eCollection 2022. Front Immunol. 2022. PMID: 36569948 Free PMC article. - Non-Melanoma Skin Cancers and Other Cutaneous Manifestations in Bone Marrow Failure Syndromes and Rare DNA Repair Disorders.
Vagher J, Gammon A, Kohlmann W, Jeter J. Vagher J, et al. Front Oncol. 2022 Mar 10;12:837059. doi: 10.3389/fonc.2022.837059. eCollection 2022. Front Oncol. 2022. PMID: 35359366 Free PMC article. Review. - Single-cell transcription profiles in Bloom syndrome patients link BLM deficiency with altered condensin complex expression signatures.
Gönenc II, Wolff A, Schmidt J, Zibat A, Müller C, Cyganek L, Argyriou L, Räschle M, Yigit G, Wollnik B. Gönenc II, et al. Hum Mol Genet. 2022 Jul 7;31(13):2185-2193. doi: 10.1093/hmg/ddab373. Hum Mol Genet. 2022. PMID: 35099000 Free PMC article. - Diagnosis of Bloom Syndrome in a Patient with Short Stature, Recurrence of Malignant Lymphoma, and Consanguineous Origin.
Trizuljak J, Petruchová T, Blaháková I, Vrzalová Z, Hořínová V, Doubková M, Michalka J, Mayer J, Pospíšilová Š, Doubek M. Trizuljak J, et al. Mol Syndromol. 2020 Jun;11(2):73-82. doi: 10.1159/000507006. Epub 2020 Mar 21. Mol Syndromol. 2020. PMID: 32655338 Free PMC article. - Gene expression profile suggesting immunological dysregulation in two Brazilian Bloom's syndrome cases.
Montenegro MM, Quaio CR, Palmeira P, Gasparini Y, Rangel-Santos A, Damasceno J, Novak EM, Gimenez TM, Yamamoto GL, Ronjo RS, Novo-Filho GM, Chehimi SN, Zanardo EA, Dias AT, Nascimento AM, Costa TVMM, Duarte AJDS, Coutinho LL, Kim CA, Kulikowski LD. Montenegro MM, et al. Mol Genet Genomic Med. 2020 Apr;8(4):e1133. doi: 10.1002/mgg3.1133. Epub 2020 Feb 19. Mol Genet Genomic Med. 2020. PMID: 32073752 Free PMC article.
References
- Ann Intern Med. 1966 Sep;65(3):487-95 - PubMed
- Science. 1965 Apr 23;148(3669):506-7 - PubMed
- J Med Educ. 1959 Apr;34(4):315-34 - PubMed
- Med Clin North Am. 1965 May;49:695-708 - PubMed
- Am J Dis Child. 1966 Dec;112(6):581-2 - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources