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Identical twin discordance for the Brachmann-de Lange syndrome revisited.
Carakushansky G, Aguiar MB, Gonçalves MR, Berthier CO, Kahn E, Carakushansky M, Pena SD. Carakushansky G, et al. Am J Med Genet. 1996 Jun 14;63(3):458-60. doi: 10.1002/(SICI)1096-8628(19960614)63:3<458::AID-AJMG8>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8737652
Achondroplasia associated with Down syndrome.
Carakushansky G, Rosembaum S, Ribeiro MG, Kahn E, Carakushansky M. Carakushansky G, et al. Am J Med Genet. 1998 May 1;77(2):168-9. doi: 10.1002/(sici)1096-8628(19980501)77:2<168::aid-ajmg12>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9605293 No abstract available.
[Partial monosomy of chromosome 13. Study of 2 cases].
Carakushansky G, Büellerback AE. Carakushansky G, et al. AMB Rev Assoc Med Bras. 1979 Nov;25(11):392-4. AMB Rev Assoc Med Bras. 1979. PMID: 317731 Portuguese. No abstract available.
Craniometaphyseal dysplasia: case report.
Maia LC, Modesto A, Carakushansky G, de Souza IP. Maia LC, et al. Among authors: carakushansky g. Braz Dent J. 2000;11(2):153-60. Braz Dent J. 2000. PMID: 11210264
Ligneous periodontitis and Ehlers-Danlos syndrome.
Pierro VS, Vazquez-Sullca R, Vieira AS, Takiya CM, Carakushansky G, Feres-Filho EJ. Pierro VS, et al. Among authors: carakushansky g. J Periodontol. 2006 Jan;77(1):123-8. doi: 10.1902/jop.2006.77.1.123. J Periodontol. 2006. PMID: 16579713
Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
Lopes-Cendes I, Teive HG, Calcagnotto ME, Da Costa JC, Cardoso F, Viana E, Maciel JA, Radvany J, Arruda WO, Trevisol-Bittencourt PC, Rosa Neto P, Silveira I, Steiner CE, Pinto Júnior W, Santos AS, Correa Neto Y, Werneck LC, Araújo AQ, Carakushansky G, Mello LR, Jardim LB, Rouleau GA. Lopes-Cendes I, et al. Among authors: carakushansky g. Arq Neuropsiquiatr. 1997 Sep;55(3B):519-29. doi: 10.1590/s0004-282x1997000400001. Arq Neuropsiquiatr. 1997. PMID: 9629399
19 results