Hendrickx J - Search Results

1

A point mutation in the FMR-1 gene associated with fragile X mental retardation.

De Boulle K, Verkerk AJ, Reyniers E, Vits L, Hendrickx J, Van Roy B, Van den Bos F, de Graaff E, Oostra BA, Willems PJ. De Boulle K, et al. Among authors: hendrickx j. Nat Genet. 1993 Jan;3(1):31-5. doi: 10.1038/ng0193-31. Nat Genet. 1993. PMID: 8490650

2

DXS89 (pTAK10) detects a homologous sequence on the Y chromosome.

Hendrickx J, Vits L, Willems PJ. Hendrickx J, et al. Genomics. 1992 Oct;14(2):554-5. doi: 10.1016/s0888-7543(05)80272-1. Genomics. 1992. PMID: 1427883 No abstract available.

3

Regional mapping of a liver alpha-subunit gene of phosphorylase kinase (PHKA) to the distal region of human chromosome Xp.

Wauters JG, Bossuyt PJ, Davidson J, Hendrickx J, Kilimann MW, Willems PJ. Wauters JG, et al. Among authors: hendrickx j. Cytogenet Cell Genet. 1992;60(3-4):194-6. doi: 10.1159/000133334. Cytogenet Cell Genet. 1992. PMID: 1505214

4

Frequency of the phenylalanine deletion (delta F508) in the CF gene of Belgian cystic fibrosis patients.

Wauters JG, Hendrickx J, Coucke P, Vits L, Stuer K, van Schil L, van der Auwera BJ, Van Elsen A, Dumon J, Willems PJ, et al. Wauters JG, et al. Among authors: hendrickx j. Clin Genet. 1991 Feb;39(2):89-92. doi: 10.1111/j.1399-0004.1991.tb02992.x. Clin Genet. 1991. PMID: 1673094

5

Mutations in the phosphorylase kinase gene PHKA2 are responsible for X-linked liver glycogen storage disease.

Hendrickx J, Coucke P, Dams E, Lee P, Odièvre M, Corbeel L, Fernandes JF, Willems PJ. Hendrickx J, et al. Hum Mol Genet. 1995 Jan;4(1):77-83. doi: 10.1093/hmg/4.1.77. Hum Mol Genet. 1995. PMID: 7711737

6

Genetic deficiencies of the glycogen phosphorylase system.

Hendrickx J, Willems PJ. Hendrickx J, et al. Hum Genet. 1996 May;97(5):551-6. doi: 10.1007/BF02281858. Hum Genet. 1996. PMID: 8655128 Review.

7

X-linked liver glycogenosis type II (XLG II) is caused by mutations in PHKA2, the gene encoding the liver alpha subunit of phosphorylase kinase.

Hendrickx J, Dams E, Coucke P, Lee P, Fernandes J, Willems PJ. Hendrickx J, et al. Hum Mol Genet. 1996 May;5(5):649-52. doi: 10.1093/hmg/5.5.649. Hum Mol Genet. 1996. PMID: 8733133

8

Positional cloning of a gene involved in hereditary multiple exostoses.

Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ. Wuyts W, et al. Among authors: hendrickx j. Hum Mol Genet. 1996 Oct;5(10):1547-57. doi: 10.1093/hmg/5.10.1547. Hum Mol Genet. 1996. PMID: 8894688

9

Identification and characterization of a novel member of the EXT gene family, EXTL2.

Wuyts W, Van Hul W, Hendrickx J, Speleman F, Wauters J, De Boulle K, Van Roy N, Van Agtmael T, Bossuyt P, Willems PJ. Wuyts W, et al. Among authors: hendrickx j. Eur J Hum Genet. 1997 Nov-Dec;5(6):382-9. Eur J Hum Genet. 1997. PMID: 9450183

10

Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.

Wuyts W, Van Hul W, De Boulle K, Hendrickx J, Bakker E, Vanhoenacker F, Mollica F, Lüdecke HJ, Sayli BS, Pazzaglia UE, Mortier G, Hamel B, Conrad EU, Matsushita M, Raskind WH, Willems PJ. Wuyts W, et al. Among authors: hendrickx j. Am J Hum Genet. 1998 Feb;62(2):346-54. doi: 10.1086/301726. Am J Hum Genet. 1998. PMID: 9463333 Free PMC article.

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