Hoogeboom AJ - Search Results

1

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Meijers-Heijboer EJ, Sandkuijl LA, Brunner HG, Smeets HJ, Hoogeboom AJ, Deelen WH, van Hemel JO, Nelen MR, Smeets DF, Niermeijer MF, et al. Meijers-Heijboer EJ, et al. Among authors: hoogeboom aj. J Med Genet. 1992 Dec;29(12):853-7. doi: 10.1136/jmg.29.12.853. J Med Genet. 1992. PMID: 1362220 Free PMC article.

2

Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosis.

van Oost BA, van Zandvoort PM, Tünte W, Brunner HG, Hoogeboom AJ, Maaswinkel-Mooy PD, Bakkeren J, Hamel B, Ropers HH. van Oost BA, et al. Among authors: hoogeboom aj. Hum Genet. 1991 Feb;86(4):404-7. doi: 10.1007/BF00201845. Hum Genet. 1991. PMID: 1671851

3

Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflex.

Peet PJ, Pereira RR, Van Hemel JO, Hoogeboom AJ. Peet PJ, et al. Among authors: hoogeboom aj. J Med Genet. 1987 Dec;24(12):786-8. doi: 10.1136/jmg.24.12.786. J Med Genet. 1987. PMID: 3430559 Free PMC article.

4

The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance.

van de Vooren MJ, Niermeijer MF, Hoogeboom AJ. van de Vooren MJ, et al. Among authors: hoogeboom aj. Clin Genet. 1983 Dec;24(6):439-45. doi: 10.1111/j.1399-0004.1983.tb00100.x. Clin Genet. 1983. PMID: 6652957

5

Prenatal diagnosis of type A1 brachydactyly.

den Hollander NS, Hoogeboom AJ, Niermeijer MF, Wladimiroff JW. den Hollander NS, et al. Among authors: hoogeboom aj. Ultrasound Obstet Gynecol. 2001 Jun;17(6):529-30. doi: 10.1046/j.1469-0705.2001.00428.x. Ultrasound Obstet Gynecol. 2001. PMID: 11422978 Free article.

6

Early prenatal sonographic diagnosis and follow-up of Jeune syndrome.

den Hollander NS, Robben SG, Hoogeboom AJ, Niermeijer MF, Wladimiroff JW. den Hollander NS, et al. Among authors: hoogeboom aj. Ultrasound Obstet Gynecol. 2001 Oct;18(4):378-83. doi: 10.1046/j.0960-7692.2001.00530.x. Ultrasound Obstet Gynecol. 2001. PMID: 11779000 Free article.

7

Clinical evidence for localisation of HLA proximal of chromosome 6p22.

Sachs ES, Hoogeboom AJ, Niermeijer MF, Schreuder GM. Sachs ES, et al. Among authors: hoogeboom aj. Lancet. 1983 Mar 19;1(8325):659. doi: 10.1016/s0140-6736(83)91839-1. Lancet. 1983. PMID: 6131344 No abstract available.

8

Chromosome studies of 500 couples with two or more abortions.

Sachs ES, Jahoda MG, Van Hemel JO, Hoogeboom AJ, Sandkuyl LA. Sachs ES, et al. Among authors: hoogeboom aj. Obstet Gynecol. 1985 Mar;65(3):375-8. Obstet Gynecol. 1985. PMID: 3974963

9

Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity alone.

Galjaard RJ, van der Ham LI, Posch NA, Dijkstra PF, Oostra BA, Hovius SE, Timmenga EJ, Sonneveld GJ, Hoogeboom AJ, Heutink P. Galjaard RJ, et al. Among authors: hoogeboom aj. Am J Med Genet. 2001 Jan 22;98(3):256-62. doi: 10.1002/1096-8628(20010122)98:3<256::aid-ajmg1088>3.0.co;2-d. Am J Med Genet. 2001. PMID: 11169564

10

Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20p.

Oegema R, van Zutven LJ, van Hassel DA, Huijbregts GC, Hoogeboom AJ. Oegema R, et al. Among authors: hoogeboom aj. Eur J Med Genet. 2012 Apr;55(4):265-8. doi: 10.1016/j.ejmg.2012.01.015. Epub 2012 Feb 21. Eur J Med Genet. 2012. PMID: 22406089

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