Sandkuyl LA - Search Results

1

Genetic heterogeneity in tuberous sclerosis.

Janssen LA, Sandkuyl LA, Merkens EC, Maat-Kievit JA, Sampson JR, Fleury P, Hennekam RC, Grosveld GC, Lindhout D, Halley DJ. Janssen LA, et al. Among authors: sandkuyl la. Genomics. 1990 Oct;8(2):237-42. doi: 10.1016/0888-7543(90)90277-2. Genomics. 1990. PMID: 1979047

2

A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23.

Janssen LA, Povey S, Attwood J, Sandkuyl LA, Lindhout D, Flodman P, Smith M, Sampson JR, Haines JL, Merkens EC, et al. Janssen LA, et al. Among authors: sandkuyl la. Ann N Y Acad Sci. 1991;615:306-15. doi: 10.1111/j.1749-6632.1991.tb37772.x. Ann N Y Acad Sci. 1991. PMID: 2039153 No abstract available.

3

Risk calculation of missed prenatal diagnosis of fragile-X syndrome.

Oostra BA, Sandkuyl LA, Halley DJ. Oostra BA, et al. Among authors: sandkuyl la. Prenat Diagn. 1990 Aug;10(8):545-6. doi: 10.1002/pd.1970100811. Prenat Diagn. 1990. PMID: 2082996 No abstract available.

4

The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis.

Halley DJ, Veeze HJ, Sandkuyl LA, Wesby-van Swaay E, van Damme NH, Deelen WH, Witte JE, Niermeijer MF. Halley DJ, et al. Among authors: sandkuyl la. Hum Genet. 1990 Sep;85(4):407-8. doi: 10.1007/BF02428281. Hum Genet. 1990. PMID: 2210750

5

Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.

Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA, et al. Wijmenga C, et al. Among authors: sandkuyl la. Genomics. 1991 Apr;9(4):570-5. doi: 10.1016/0888-7543(91)90348-i. Genomics. 1991. PMID: 2037288

6

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18.

Heutink P, van de Wetering BJ, Breedveld GJ, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA. Heutink P, et al. Among authors: sandkuyl la. J Med Genet. 1990 Jul;27(7):433-6. doi: 10.1136/jmg.27.7.433. J Med Genet. 1990. PMID: 2395161 Free PMC article.

7

[Prenatal diagnosis of cystic fibrosis using DNA analysis].

Halley DJ, Morreau J, Neijens HJ, van Swaay E, Sandkuyl LA, Oostra BA. Halley DJ, et al. Among authors: sandkuyl la. Ned Tijdschr Geneeskd. 1986 Dec 13;130(50):2270-2. Ned Tijdschr Geneeskd. 1986. PMID: 3027590 Dutch. No abstract available.

8

Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.

Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F. Kwan SP, et al. Among authors: sandkuyl la. Genomics. 1990 Feb;6(2):238-42. doi: 10.1016/0888-7543(90)90562-9. Genomics. 1990. PMID: 2307467

9

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.

Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS. Kwan SP, et al. Among authors: sandkuyl la. Genomics. 1988 Jul;3(1):39-43. doi: 10.1016/0888-7543(88)90156-5. Genomics. 1988. PMID: 2906042

10

A leucine-to-proline mutation in the insulin receptor in a family with insulin resistance.

Klinkhamer MP, Groen NA, van der Zon GC, Lindhout D, Sandkuyl LA, Krans HM, Möller W, Maassen JA. Klinkhamer MP, et al. Among authors: sandkuyl la. EMBO J. 1989 Sep;8(9):2503-7. doi: 10.1002/j.1460-2075.1989.tb08387.x. EMBO J. 1989. PMID: 2479553 Free PMC article.

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