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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: wajntal a. 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.
Chromosome aberrations in Sotos syndrome.
Wajntal A, Koiffmann CP. Wajntal A, et al. Clin Genet. 1991 Dec;40(6):472. Clin Genet. 1991. PMID: 1817484 No abstract available.
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. Am J Med Genet. 1985 Feb;20(2):265-9. doi: 10.1002/ajmg.1320200209. Am J Med Genet. 1985. PMID: 3976719
Macrosomia, obesity, macrocephaly and ocular abnormalities (MOMO syndrome) in two unrelated patients: delineation of a newly recognized overgrowth syndrome.
Moretti-Ferreira D, Koiffmann CP, Listik M, Setian N, Wajntal A. Moretti-Ferreira D, et al. Among authors: wajntal a. Am J Med Genet. 1993 Jun 15;46(5):555-8. doi: 10.1002/ajmg.1320460519. Am J Med Genet. 1993. PMID: 8322820
Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11.
Koiffmann CP, de Souza DH, Diament A, Ventura HB, Alves RS, Kihara S, Wajntal A. Koiffmann CP, et al. Among authors: wajntal a. Am J Med Genet. 1993 Jun 15;46(5):529-33. doi: 10.1002/ajmg.1320460514. Am J Med Genet. 1993. PMID: 8322815 Review.
Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
Koiffmann CP, Gonzalez CH, Vianna-Morgante AM, Kim CA, Odone-Filho V, Wajntal A. Koiffmann CP, et al. Among authors: wajntal a. Am J Med Genet. 1995 Jul 31;58(1):46-9. doi: 10.1002/ajmg.1320580110. Am J Med Genet. 1995. PMID: 7573155 Review.
Pathologic findings in the Wolf-Hirschhorn (4p-) syndrome.
Gonzalez CH, Capelozzi VL, Wajntal A. Gonzalez CH, et al. Among authors: wajntal a. Am J Med Genet. 1981;9(3):183-7. doi: 10.1002/ajmg.1320090303. Am J Med Genet. 1981. PMID: 7282779 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. Among authors: wajntal a. Am J Med Genet. 1983 Jan;14(1):159-67. doi: 10.1002/ajmg.1320140122. Am J Med Genet. 1983. PMID: 6829605
Familial recurrence of geleophysic dysplasia.
Koiffmann CP, Wajntal A, Ursich MJ, Pupo AA. Koiffmann CP, et al. Among authors: wajntal a. Am J Med Genet. 1984 Nov;19(3):483-6. doi: 10.1002/ajmg.1320190309. Am J Med Genet. 1984. PMID: 6507494
Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
Koiffmann CP, Wajntal A, Huyke BJ, Castro RM. Koiffmann CP, et al. Among authors: wajntal a. Am J Med Genet. 1988 Feb;29(2):263-8. doi: 10.1002/ajmg.1320290203. Am J Med Genet. 1988. PMID: 3354597
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