Opitz JM - Search Results

1

An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome.

Jehee FS, Rosenberg C, Krepischi-Santos AC, Kok F, Knijnenburg J, Froyen G, Vianna-Morgante AM, Opitz JM, Passos-Bueno MR. Jehee FS, et al. Among authors: opitz jm. Am J Med Genet A. 2005 Dec 15;139(3):221-6. doi: 10.1002/ajmg.a.30991. Am J Med Genet A. 2005. PMID: 16283679

2

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: opitz jm. Am J Med Genet. 1990 Oct;37(2):213-23. doi: 10.1002/ajmg.1320370210. Am J Med Genet. 1990. PMID: 2248288

3

FG syndrome update 1988: note of 5 new patients and bibliography.

Opitz JM, Richieri-da Costa A, Aase JM, Benke PJ. Opitz JM, et al. Am J Med Genet. 1988 May-Jun;30(1-2):309-28. doi: 10.1002/ajmg.1320300132. Am J Med Genet. 1988. PMID: 3052062 Review.

4

Simpson-Golabi-Behmel syndrome: an X-linked encephalo-tropho-schisis syndrome.

Neri G, Marini R, Cappa M, Borrelli P, Opitz JM. Neri G, et al. Among authors: opitz jm. Am J Med Genet. 1988 May-Jun;30(1-2):287-99. doi: 10.1002/ajmg.1320300130. Am J Med Genet. 1988. PMID: 3177455

5

Sensorineural deafness in the FG syndrome: report on four new cases.

Neri G, Blumberg B, Miles PV, Opitz JM. Neri G, et al. Among authors: opitz jm. Am J Med Genet. 1984 Oct;19(2):369-77. doi: 10.1002/ajmg.1320190219. Am J Med Genet. 1984. PMID: 6542310

6

Encomium: Oswaldo Frota-Pessoa.

Vianna-Morgante AM, Azevêdo ES, Otto PA, Opitz JM. Vianna-Morgante AM, et al. Among authors: opitz jm. Am J Med Genet. 1996 Jun 28;63(4):581-4. doi: 10.1002/(SICI)1096-8628(19960628)63:4<581::AID-AJMG12>3.0.CO;2-E. Am J Med Genet. 1996. PMID: 8826438 No abstract available.

7

FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3].

Dessay S, Moizard MP, Gilardi JL, Opitz JM, Middleton-Price H, Pembrey M, Moraine C, Briault S. Dessay S, et al. Among authors: opitz jm. Am J Med Genet. 2002 Sep 15;112(1):6-11. doi: 10.1002/ajmg.10546. Am J Med Genet. 2002. PMID: 12239712 Review.

8

Genetics of tethered cord "syndrome": The FG syndrome.

Opitz JM. Opitz JM. Am J Med Genet A. 2005 Feb 1;132A(4):454-5. doi: 10.1002/ajmg.a.30440. Am J Med Genet A. 2005. PMID: 15551262 No abstract available.

9

X-linked congenital ataxia: a new locus maps to Xq25-q27.1.

Zanni G, Bertini E, Bellcross C, Nedelec B, Froyen G, Neuhäuser G, Opitz JM, Chelly J. Zanni G, et al. Among authors: opitz jm. Am J Med Genet A. 2008 Mar 1;146A(5):593-600. doi: 10.1002/ajmg.a.32186. Am J Med Genet A. 2008. PMID: 18241076

10

A previously undescribed syndrome combining fibular agenesis/hypoplasia, oligodactylous clubfeet, anonychia/ungual hypoplasia, and other defects.

Santos SC, Pardono E, Ferreira da Costa MI, de Melo AN, Graciani Z, de Albuquerque e Souza AC, Lezirovitz K, Thiele-Aguiar RS, Mingroni-Netto RC, Opitz JM, Kok F, Otto PA. Santos SC, et al. Among authors: opitz jm. Am J Med Genet A. 2008 Dec 15;146A(24):3126-31. doi: 10.1002/ajmg.a.32580. Am J Med Genet A. 2008. PMID: 19012338

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