Fryns JP - Search Results

1

Genetic locus on chromosome 6p for multicystic renal dysplasia, pelvi-ureteral junction stenosis, and vesicoureteral reflux.

Devriendt K, Fryns JP. Devriendt K, et al. Among authors: fryns jp. Am J Med Genet. 1995 Nov 20;59(3):396-8. doi: 10.1002/ajmg.1320590326. Am J Med Genet. 1995. PMID: 8599371 No abstract available.

2

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly.

Dimitrov BI, Voet T, De Smet L, Vermeesch JR, Devriendt K, Fryns JP, Debeer P. Dimitrov BI, et al. Among authors: fryns jp. J Med Genet. 2010 Aug;47(8):569-74. doi: 10.1136/jmg.2009.073833. Epub 2010 Jul 7. J Med Genet. 2010. PMID: 20610440

3

2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.

Dimitrov B, Balikova I, de Ravel T, Van Esch H, De Smedt M, Baten E, Vermeesch JR, Bradinova I, Simeonov E, Devriendt K, Fryns JP, Debeer P. Dimitrov B, et al. Among authors: fryns jp. J Med Genet. 2011 Feb;48(2):98-104. doi: 10.1136/jmg.2010.079491. Epub 2010 Nov 10. J Med Genet. 2011. PMID: 21068127

4

Glypican 1 gene: good candidate for brachydactyly type E.

Syrrou M, Keymolen K, Devriendt K, Holvoet M, Thoelen R, Verhofstadt K, Fryns JP. Syrrou M, et al. Among authors: fryns jp. Am J Med Genet. 2002 Apr 1;108(4):310-4. doi: 10.1002/ajmg.10266. Am J Med Genet. 2002. PMID: 11920836

5

Mosaic trisomy 8 as a cause of velopharyngeal insufficiency.

Vantrappen G, Rommel N, Cremers CW, Fryns JP, Devriendt K. Vantrappen G, et al. Among authors: fryns jp. Am J Med Genet. 2002 Apr 1;108(4):337-8. doi: 10.1002/ajmg.10270. Am J Med Genet. 2002. PMID: 11920842 No abstract available.

6

Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.

Devriendt K, D'Espallier L, Fryns JP. Devriendt K, et al. Among authors: fryns jp. J Med Genet. 1996 Mar;33(3):224-6. doi: 10.1136/jmg.33.3.224. J Med Genet. 1996. PMID: 8728696 Free PMC article.

7

Renal and urological tract malformations caused by a 22q11 deletion.

Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M. Devriendt K, et al. Among authors: fryns jp. J Med Genet. 1996 Apr;33(4):349. doi: 10.1136/jmg.33.4.349. J Med Genet. 1996. PMID: 8730297 Free PMC article. No abstract available.

8

Velo-facio-skeletal syndrome versus Aarskog syndrome.

Fryns JP, Devriendt K. Fryns JP, et al. Am J Med Genet. 1996 Sep 6;64(4):604. doi: 10.1002/ajmg.1320640403. Am J Med Genet. 1996. PMID: 8870930 No abstract available.

9

Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia.

Groenen PM, Garcia E, Debeer P, Devriendt K, Fryns JP, Van de Ven WJ. Groenen PM, et al. Among authors: fryns jp. Genomics. 1996 Dec 1;38(2):141-8. doi: 10.1006/geno.1996.0609. Genomics. 1996. PMID: 8954795

10

Isolation of cosmids corresponding to the chromosome breakpoints of a de novo autosomal translocation, t(6;19)(p21;q13.1), in a patient with multicystic renal dysplasia.

Groenen PM, Garcia E, Thoelen R, Aly M, Schoenmakers EF, Devriendt K, Fryns JP, Van de Ven WJ. Groenen PM, et al. Among authors: fryns jp. Cytogenet Cell Genet. 1996;75(4):210-5. doi: 10.1159/000134485. Cytogenet Cell Genet. 1996. PMID: 9067426

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