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Human situs determination and chromosome constitution 46,XY,ins(7;8)(q22;q12q24).
Koiffmann CP, Wajntal A, de Souza DH, Gonzalez CH, Coates MV. Koiffmann CP, et al. Among authors: gonzalez ch. Am J Med Genet. 1993 Sep 15;47(4):568-9. doi: 10.1002/ajmg.1320470426. Am J Med Genet. 1993. PMID: 8192752 No abstract available.
Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12).
Gonzalez CH, Billerbeck AE, Takayama LC, Wajntal A. Gonzalez CH, et al. Am J Med Genet. 1983 Jan;14(1):159-67. doi: 10.1002/ajmg.1320140122. Am J Med Genet. 1983. PMID: 6829605
Brief cytogenetic report on maternal translocation t(7;9) (p22:p13): two sibs with duplication 9p and one sib with the balanced translocation.
Wajntal A, Gonzalez CH, Koiffmann CP, de Souza DH. Wajntal A, et al. Among authors: gonzalez ch. Am J Med Genet. 1985 Feb;20(2):265-9. doi: 10.1002/ajmg.1320200209. Am J Med Genet. 1985. PMID: 3976719
Pathologic findings in the Wolf-Hirschhorn (4p-) syndrome.
Gonzalez CH, Capelozzi VL, Wajntal A. Gonzalez CH, et al. Am J Med Genet. 1981;9(3):183-7. doi: 10.1002/ajmg.1320090303. Am J Med Genet. 1981. PMID: 7282779 No abstract available.
Caudal "regression" anomaly in a boy born to a pancreatectomized mother.
Gonzalez CH, Sadeck LS, Kim CA, Leone CR, Ramos JL, Barba MF, Monaci J, Machado MC. Gonzalez CH, et al. Am J Med Genet. 1985 May;21(1):205-9. doi: 10.1002/ajmg.1320210131. Am J Med Genet. 1985. PMID: 4003445 No abstract available.
Are Noonan syndrome and Noonan-like/multiple giant cell lesion syndrome distinct entities?
Bertola DR, Kim CA, Pereira AC, Mota GF, Krieger JE, Vieira IC, Valente M, Loreto MR, Magalhães RP, Gonzalez CH. Bertola DR, et al. Among authors: gonzalez ch. Am J Med Genet. 2001 Jan 22;98(3):230-4. doi: 10.1002/1096-8628(20010122)98:3<230::aid-ajmg1080>3.0.co;2-k. Am J Med Genet. 2001. PMID: 11169560
Brief clinical report: chondroectodermal dysplasia (Ellis-van Creveld) with anomalies of CNS and urinary tract.
Rosemberg S, Carneiro PC, Zerbini MC, Gonzalez CH. Rosemberg S, et al. Among authors: gonzalez ch. Am J Med Genet. 1983 Jun;15(2):291-5. doi: 10.1002/ajmg.1320150212. Am J Med Genet. 1983. PMID: 6881201
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology.
Whitley CB, Langer LO Jr, Ophoven J, Gilbert EF, Gonzalez CH, Mammel M, Coleman M, Rosemberg S, Rodriques CJ, Sibley R, et al. Whitley CB, et al. Among authors: gonzalez ch. Am J Med Genet. 1984 Oct;19(2):265-75. doi: 10.1002/ajmg.1320190209. Am J Med Genet. 1984. PMID: 6507478
Creatine-kinase and pyruvate-kinase activities in normal children: implications in Duchenne muscular dystrophy carrier detection.
Passos MR, Gonzalez CH, Zatz M. Passos MR, et al. Among authors: gonzalez ch. Am J Med Genet. 1985 Oct;22(2):255-62. doi: 10.1002/ajmg.1320220206. Am J Med Genet. 1985. PMID: 4050856
GAPO syndrome: report of three affected brothers.
Gagliardi AR, González CH, Pratesi R. Gagliardi AR, et al. Among authors: gonzalez ch. Am J Med Genet. 1984 Oct;19(2):217-23. doi: 10.1002/ajmg.1320190203. Am J Med Genet. 1984. PMID: 6507472
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