Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

58 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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. 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.
A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome.
Pacanaro AN, Christofolini DM, Kulikowski LD, Belangero SI, da Silva Bellucco FT, Varela MC, Koiffmann CP, Yoshimoto M, Squire JA, Schiavon AV, Heck B, Melaragno MI. Pacanaro AN, et al. Among authors: koiffmann cp. Am J Med Genet A. 2010 Mar;152A(3):753-8. doi: 10.1002/ajmg.a.33308. Am J Med Genet A. 2010. PMID: 20186782
MLPA analysis in 30 Sotos syndrome patients revealed one total NSD1 deletion and two partial deletions not previously reported.
Fagali C, Kok F, Nicola P, Kim C, Bertola D, Albano L, Koiffmann CP. Fagali C, et al. Among authors: koiffmann cp. Eur J Med Genet. 2009 Sep-Oct;52(5):333-6. doi: 10.1016/j.ejmg.2009.07.001. Epub 2009 Jul 9. Eur J Med Genet. 2009. PMID: 19596467
Chromosome aberrations in Sotos syndrome.
Wajntal A, Koiffmann CP. Wajntal A, et al. Among authors: koiffmann cp. Clin Genet. 1991 Dec;40(6):472. Clin Genet. 1991. PMID: 1817484 No abstract available.
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: koiffmann cp. 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. 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. Am J Med Genet. 1995 Jul 31;58(1):46-9. doi: 10.1002/ajmg.1320580110. Am J Med Genet. 1995. PMID: 7573155 Review.
Familial recurrence of geleophysic dysplasia.
Koiffmann CP, Wajntal A, Ursich MJ, Pupo AA. Koiffmann CP, et al. Am J Med Genet. 1984 Nov;19(3):483-6. doi: 10.1002/ajmg.1320190309. Am J Med Genet. 1984. PMID: 6507494
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: koiffmann cp. Am J Med Genet. 1985 Feb;20(2):265-9. doi: 10.1002/ajmg.1320200209. Am J Med Genet. 1985. PMID: 3976719
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. Am J Med Genet. 1988 Feb;29(2):263-8. doi: 10.1002/ajmg.1320290203. Am J Med Genet. 1988. PMID: 3354597
58 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback