Höweler CJ - Search Results

1

Brief report: reverse mutation in myotonic dystrophy.

Brunner HG, Jansen G, Nillesen W, Nelen MR, de Die CE, Höweler CJ, van Oost BA, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. Among authors: howeler cj. N Engl J Med. 1993 Feb 18;328(7):476-80. doi: 10.1056/NEJM199302183280705. N Engl J Med. 1993. PMID: 8421477 Free article. No abstract available.

2

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Jansen G, Willems P, Coerwinkel M, Nillesen W, Smeets H, Vits L, Höweler C, Brunner H, Wieringa B. Jansen G, et al. Am J Hum Genet. 1994 Apr;54(4):575-85. Am J Hum Genet. 1994. PMID: 8128954 Free PMC article.

3

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Brunner HG, Brüggenwirth HT, Nillesen W, Jansen G, Hamel BC, Hoppe RL, de Die CE, Höweler CJ, van Oost BA, Wieringa B, et al. Brunner HG, et al. Among authors: howeler cj. Am J Hum Genet. 1993 Nov;53(5):1016-23. Am J Hum Genet. 1993. PMID: 8213829 Free PMC article.

4

[An unstable mutation as cause of myotonic dystrophy].

Brunner HG, Höweler CJ, Smeets HJ, Wieringa B. Brunner HG, et al. Among authors: howeler cj. Ned Tijdschr Geneeskd. 1993 Nov 27;137(48):2468-72. Ned Tijdschr Geneeskd. 1993. PMID: 8272119 Review. Dutch. No abstract available.

5

Intestinal pseudo-obstruction in myotonic dystrophy.

Brunner HG, Hamel BC, Rieu P, Höweler CJ, Peters FT. Brunner HG, et al. Among authors: howeler cj. J Med Genet. 1992 Nov;29(11):791-3. doi: 10.1136/jmg.29.11.791. J Med Genet. 1992. PMID: 1453429 Free PMC article.

6

Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family.

de Die-Smulders CE, Höweler CJ, Mirandolle JF, Brunner HG, Hovers V, Brüggenwirth H, Smeets HJ, Geraedts JP. de Die-Smulders CE, et al. Among authors: howeler cj. J Med Genet. 1994 Aug;31(8):595-601. doi: 10.1136/jmg.31.8.595. J Med Genet. 1994. PMID: 7815415 Free PMC article.

7

Paternal transmission of congenital myotonic dystrophy.

de Die-Smulders CE, Smeets HJ, Loots W, Anten HB, Mirandolle JF, Geraedts JP, Höweler CJ. de Die-Smulders CE, et al. Among authors: howeler cj. J Med Genet. 1997 Nov;34(11):930-3. doi: 10.1136/jmg.34.11.930. J Med Genet. 1997. PMID: 9391889 Free PMC article.

8

Age and causes of death in adult-onset myotonic dystrophy.

de Die-Smulders CE, Höweler CJ, Thijs C, Mirandolle JF, Anten HB, Smeets HJ, Chandler KE, Geraedts JP. de Die-Smulders CE, et al. Among authors: howeler cj. Brain. 1998 Aug;121 ( Pt 8):1557-63. doi: 10.1093/brain/121.8.1557. Brain. 1998. PMID: 9712016

9

Anticipation in myotonic dystrophy: fact or fiction?

Höweler CJ, Busch HF, Geraedts JP, Niermeijer MF, Staal A. Höweler CJ, et al. Brain. 1989 Jun;112 ( Pt 3):779-97. doi: 10.1093/brain/112.3.779. Brain. 1989. PMID: 2731029

10

X-linked mental retardation and neurological symptoms: a nosological approach.

Schrander-Stumpel CT, Höweler CJ, Fryns JP. Schrander-Stumpel CT, et al. Among authors: howeler cj. Genet Couns. 1995;6(1):21-32. Genet Couns. 1995. PMID: 7794558 Review.

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