Koiffmann CP - Search Results

1

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.

2

[Macrosomia, macrocrania and motor disorders in childhood, Sotos syndrome (McKusick 11755): report of 7 cases and review of clinical aspects of 198 reported cases].

Moretti-Ferreira D, Koiffmann CP, Wajntal A, Diament AJ, De Mendonça BB, Mattieli J, Saldanha PH. Moretti-Ferreira D, et al. Among authors: koiffmann cp. Arq Neuropsiquiatr. 1991 Jun;49(2):164-71. doi: 10.1590/s0004-282x1991000200009. Arq Neuropsiquiatr. 1991. PMID: 1810234 Portuguese.

3

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.

4

Is Shwachman syndrome (McKusick 26040) a chromosome breakage syndrome?

Koiffmann CP, Gonzalez CH, Souza DH, Romani EG, Kim CA, Wajntal A. Koiffmann CP, et al. Hum Genet. 1991 May;87(1):106-7. doi: 10.1007/BF01213107. Hum Genet. 1991. PMID: 2037277 No abstract available.

5

GAPO syndrome (McKusick 23074)--a connective tissue disorder: report on two affected sibs and on the pathologic findings in the older.

Wajntal A, Koiffmann CP, Mendonça BB, Epps-Quaglia D, Sotto MN, Rati PB, Opitz JM. Wajntal A, et al. Among authors: koiffmann cp. Am J Med Genet. 1990 Oct;37(2):213-23. doi: 10.1002/ajmg.1320370210. Am J Med Genet. 1990. PMID: 2248288

6

Ring chromosome 7 in a man with multiple congenital anomalies and mental retardation.

Koiffmann CP, Diament A, de Souza DH, Wajntal A. Koiffmann CP, et al. J Med Genet. 1990 Jul;27(7):462-4. doi: 10.1136/jmg.27.7.462. J Med Genet. 1990. PMID: 2395166 Free PMC article.

7

Macrocephaly, multiple lipomas, and hemangiomata (Bannayan-Zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms?

Moretti-Ferreira D, Koiffmann CP, Souza DH, Diament AJ, Wajntal A. Moretti-Ferreira D, et al. Among authors: koiffmann cp. Am J Med Genet. 1989 Dec;34(4):548-51. doi: 10.1002/ajmg.1320340419. Am J Med Genet. 1989. PMID: 2624267

8

[Role of chromosome changes in the etiology of male infertility].

Soares-Vieira JA, Wajntal A, Koiffmann CP. Soares-Vieira JA, et al. Among authors: koiffmann cp. Rev Paul Med. 1988 May-Jun;106(3):150-4. Rev Paul Med. 1988. PMID: 3251346 Portuguese. No abstract available.

9

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

10

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

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