Dagan J - Search Results

1

Cytogenetic investigations in families with ataxia-telangiectasia.

Cohen MM, Shaham M, Dagan J, Shmueli E, Kohn G. Cohen MM, et al. Among authors: dagan j. Cytogenet Cell Genet. 1975;15(5):338-56. doi: 10.1159/000130530. Cytogenet Cell Genet. 1975. PMID: 1222588

2

Partial trisomy D: a diagnostic and cytogenetic dilemma.

Cohen MM, Rosenmann A, Dagan J, Legum C. Cohen MM, et al. Among authors: dagan j. J Med Genet. 1976 Dec;13(6):535-8. doi: 10.1136/jmg.13.6.535. J Med Genet. 1976. PMID: 1018316 Free PMC article.

3

A long unidentifiable extra chromosomal segment--a possible duplication of human 7q.

Wahrman J, Cohen MM, Rosenmann A, Goitein R, Richler C, Dagan J. Wahrman J, et al. Among authors: dagan j. Cytogenet Cell Genet. 1978;20(1-6):160-8. doi: 10.1159/000130848. Cytogenet Cell Genet. 1978. PMID: 648175

4

Chromosome deletion (46, XY, 20q-) in sideroblastic anemia.

Cohen MM, Ariel I, Dagan J. Cohen MM, et al. Among authors: dagan j. Isr J Med Sci. 1974 Nov;10(11):1393-6. Isr J Med Sci. 1974. PMID: 4443214 No abstract available.

5

Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-3pter syndrome.

Reifen RM, Gale R, Kerem E, Armon Y, Brand A, Dagan J, Kohn G. Reifen RM, et al. Among authors: dagan j. Clin Genet. 1986 Aug;30(2):127-30. doi: 10.1111/j.1399-0004.1986.tb00581.x. Clin Genet. 1986. PMID: 3757303

6

The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23.

Ziv Y, Rotman G, Frydman M, Dagan J, Cohen T, Foroud T, Gatti RA, Shiloh Y. Ziv Y, et al. Among authors: dagan j. Genomics. 1991 Feb;9(2):373-5. doi: 10.1016/0888-7543(91)90268-j. Genomics. 1991. PMID: 1672297

7

A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.

Voss R, Gross-Kieselstein E, Hurvitz H, Dagan J, Kerem E, Zlotogora J. Voss R, et al. Among authors: dagan j. J Med Genet. 1984 Dec;21(6):454-9. doi: 10.1136/jmg.21.6.454. J Med Genet. 1984. PMID: 6512835 Free PMC article.

8

t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.

Abeliovich D, Dagan J, Lerer I, Silberstein S, Katznelson MB, Frydman M. Abeliovich D, et al. Among authors: dagan j. Am J Med Genet. 1996 Dec 2;66(1):45-51. doi: 10.1002/(SICI)1096-8628(19961202)66:1<45::AID-AJMG10>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8957510

9

Isochromosome 18p in a mother and her child.

Abeliovich D, Dagan J, Levy A, Steinberg A, Zlotogora J. Abeliovich D, et al. Among authors: dagan j. Am J Med Genet. 1993 Jun 1;46(4):392-3. doi: 10.1002/ajmg.1320460409. Am J Med Genet. 1993. PMID: 8357009

10

The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literature.

Raas-Rothschild A, Dijkhuizen T, Sikkema-Raddatz B, Werner M, Dagan J, Abeliovich D, Lerer I. Raas-Rothschild A, et al. Among authors: dagan j. Eur J Med Genet. 2009 Mar-Jun;52(2-3):140-4. doi: 10.1016/j.ejmg.2009.03.011. Epub 2009 Mar 26. Eur J Med Genet. 2009. PMID: 19328248 Review.

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