Fekrvand S, Abolhassani H, Esfahani Z, Fard N, Amiri M, Salehi H
J Clin Immunol. 2024; 45(1):34.
PMID: 39466473
DOI: 10.1007/s10875-024-01810-w.
Samir P, Kanneganti T
Cells. 2022; 11(10).
PMID: 35626643
PMC: 9139286.
DOI: 10.3390/cells11101608.
Dhar S, Brosh R
Cell Cycle. 2018; 17(18):2207-2220.
PMID: 30209988
PMC: 6226233.
DOI: 10.1080/15384101.2018.1520567.
Al Kaissi A, Kuranova M, Pleskach N, Kenis V, Nassib N, Grill F
Medicine (Baltimore). 2018; 96(50):e8970.
PMID: 29390291
PMC: 5815703.
DOI: 10.1097/MD.0000000000008970.
Warren S, Schultz R, Chang C, Wade M, Trosko J
Proc Natl Acad Sci U S A. 1981; 78(5):3133-7.
PMID: 6942420
PMC: 319514.
DOI: 10.1073/pnas.78.5.3133.
Family exhibiting cerebellar-like ataxia, photosensitivity and shortness of stature - a new inborn error of tryptophan metabolism.
Fenton D, Wilkinson J, Toseland P
J R Soc Med. 1983; 76(9):736-9.
PMID: 6620277
PMC: 1439397.
DOI: 10.1177/014107688307600906.
Bloom's syndrome: case report.
Manning D, Fennelly J, CAHALANE S, Gill D
Ir J Med Sci. 1983; 152(2):108-10.
PMID: 6573304
DOI: 10.1007/BF02961042.
Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients.
German J
Am J Hum Genet. 1969; 21(2):196-227.
PMID: 5770175
PMC: 1706430.
Intrauterine growth retardation.
Chandra R
Indian J Pediatr. 1967; 34(233):216-8.
PMID: 5627911
Immunological development and antibody deficiency diseases.
Br Med J. 1967; 1(5536):320-1.
PMID: 5334746
PMC: 1840799.
DOI: 10.1136/bmj.1.5536.320-a.
Further studies on experimental benzene induced aplastic anemia.
Kissling M, Speck B
Blut. 1972; 25(2):97-103.
PMID: 5050160
DOI: 10.1007/BF01633873.
[Bloom's syndrome].
Kirchner M, Hesse V
Humangenetik. 1972; 15(1):25-32.
PMID: 5046905
DOI: 10.1007/BF00273428.
Diseases of Jews.
Krikler D
Postgrad Med J. 1970; 46(542):687-97.
PMID: 4923893
PMC: 2467115.
DOI: 10.1136/pgmj.46.542.687.
[Cytogenetic studies following chronic exposure to benzene (author's transl)].
Khan H, Khan M
Arch Toxikol. 1973; 31(1):39-49.
PMID: 4747544
[Cytogenetic, immunological and cytological family studies in Bloom's syndrome].
KEUTEL J
Humangenetik. 1969; 8(2):142-57.
PMID: 4189096
DOI: 10.1007/BF00295838.
Presence of abnormally high incidences of sister chromatid exchanges in three successive cell cycles in Bloom's syndrome lymphocytes.
Tsuji H, Kojima T
Chromosoma. 1985; 93(1):87-93.
PMID: 4064833
DOI: 10.1007/BF01259450.
Immunological lesions in human uracil DNA glycosylase: association with Bloom syndrome.
Seal G, Brech K, Karp S, Cool B, Sirover M
Proc Natl Acad Sci U S A. 1988; 85(7):2339-43.
PMID: 3353381
PMC: 279987.
DOI: 10.1073/pnas.85.7.2339.
Elevated sister chromatid exchange phenotype of Bloom syndrome cells is complemented by human chromosome 15.
McDaniel L, Schultz R
Proc Natl Acad Sci U S A. 1992; 89(17):7968-72.
PMID: 1518822
PMC: 49836.
DOI: 10.1073/pnas.89.17.7968.
Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.
German J, Bloom D, Passarge E, Fried K, Goodman R, KATZENELLENBOGEN I
Am J Hum Genet. 1977; 29(6):553-62.
PMID: 930922
PMC: 1685519.
Endocrine abnormalities and myopathy in Bloom's syndrome.
Ahmad U, Fisher E, Danowski T, Nolan S, Stephan T
J Med Genet. 1977; 14(6):418-21.
PMID: 604492
PMC: 1013637.
DOI: 10.1136/jmg.14.6.418.