Opitz JM - Search Results

1

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.

2

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.

3

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

4

The neurofaciodigitorenal (NFDR) syndrome.

Freire-Maia N, Pinheiro M, Opitz JM. Freire-Maia N, et al. Among authors: opitz jm. Am J Med Genet. 1982 Mar;11(3):329-36. doi: 10.1002/ajmg.1320110309. Am J Med Genet. 1982. PMID: 7081297

5

Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature.

Robin NH, Opitz JM, Muenke M. Robin NH, et al. Among authors: opitz jm. Am J Med Genet. 1996 Mar 29;62(3):305-17. doi: 10.1002/(SICI)1096-8628(19960329)62:3<305::AID-AJMG20>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8882794 No abstract available.

6

Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndrome.

Rauch A, Feindt KA, Leonard CO, Thompson JA, Hoffman RO, Creel DJ, Opitz JM. Rauch A, et al. Among authors: opitz jm. Am J Med Genet. 1999 Jan 15;82(2):194-8. doi: 10.1002/(sici)1096-8628(19990115)82:2<194::aid-ajmg18>3.0.co;2-7. Am J Med Genet. 1999. PMID: 9934988

7

Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndrome.

Gurrieri F, Scarano G, Garavelli L, Della Monica M, Lonardo F, Cuda D, Banchini G, Opitz JM, Neri G. Gurrieri F, et al. Among authors: opitz jm. Am J Med Genet A. 2004 Apr 15;126A(2):204-7. doi: 10.1002/ajmg.a.20575. Am J Med Genet A. 2004. PMID: 15057987

8

Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations.

So J, Suckow V, Kijas Z, Kalscheuer V, Moser B, Winter J, Baars M, Firth H, Lunt P, Hamel B, Meinecke P, Moraine C, Odent S, Schinzel A, van der Smagt JJ, Devriendt K, Albrecht B, Gillessen-Kaesbach G, van der Burgt I, Petrij F, Faivre L, McGaughran J, McKenzie F, Opitz JM, Cox T, Schweiger S. So J, et al. Among authors: opitz jm. Am J Med Genet A. 2005 Jan 1;132A(1):1-7. doi: 10.1002/ajmg.a.30407. Am J Med Genet A. 2005. PMID: 15558842

9

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

10

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

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