Hoovers J - Search Results

1

LEOPARD syndrome with partly normal skin and sex chromosome mosaicism.

Writzl K, Hoovers J, Sistermans EA, Hennekam RC. Writzl K, et al. Among authors: hoovers j. Am J Med Genet A. 2007 Nov 1;143A(21):2612-5. doi: 10.1002/ajmg.a.31991. Am J Med Genet A. 2007. PMID: 17935252

2

Further delineation of the chromosome 14q terminal deletion syndrome.

van Karnebeek CD, Quik S, Sluijter S, Hulsbeek MM, Hoovers JM, Hennekam RC. van Karnebeek CD, et al. Among authors: hoovers jm. Am J Med Genet. 2002 Jun 1;110(1):65-72. doi: 10.1002/ajmg.10207. Am J Med Genet. 2002. PMID: 12116274 Review.

3

Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndrome.

Mathijssen IB, Hoovers JM, Mul AN, Man HY, Ket JL, Hennekam RC. Mathijssen IB, et al. Among authors: hoovers jm. Am J Med Genet A. 2005 Jul 1;136(1):76-80. doi: 10.1002/ajmg.a.30758. Am J Med Genet A. 2005. PMID: 15889415

4

Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.

van Karnebeek CD, Koevoets C, Sluijter S, Bijlsma EK, Smeets DF, Redeker EJ, Hennekam RC, Hoovers JM. van Karnebeek CD, et al. Among authors: hoovers jm. J Med Genet. 2002 Aug;39(8):546-53. doi: 10.1136/jmg.39.8.546. J Med Genet. 2002. PMID: 12161591 Free PMC article.

5

Familial cryptic translocation between chromosomes 2qter and 8qter: further delineation of the Albright hereditary osteodystrophy-like phenotype.

Bijlsma EK, Aalfs CM, Sluitjer S, Oude Luttikhuis ME, Trembath RC, Hoovers JM, Hennekam RC. Bijlsma EK, et al. Among authors: hoovers jm. J Med Genet. 1999 Aug;36(8):604-9. J Med Genet. 1999. PMID: 10465110 Free PMC article.

6

Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.

van Langen IM, Otter MA, Aronson DC, Overweg-Plandsoen WC, Hennekam RC, Leschot NJ, Hoovers JM. van Langen IM, et al. Among authors: hoovers jm. Clin Genet. 1996 Jan;49(1):49-53. doi: 10.1111/j.1399-0004.1996.tb04325.x. Clin Genet. 1996. PMID: 8721573

7

Further delineation of the partial proximal trisomy 10q syndrome.

Aalfs CM, Hoovers JM, Nieste-Otter MA, Mannens MM, Hennekam RC, Leschot NJ. Aalfs CM, et al. Among authors: hoovers jm. J Med Genet. 1995 Dec;32(12):968-71. doi: 10.1136/jmg.32.12.968. J Med Genet. 1995. PMID: 8825926 Free PMC article.

8

Two supernumerary marker chromosomes, derived from chromosome 6 and 9, in a boy with mild developmental delay.

Aalfs CM, Jacobs ME, Nieste-Otter MA, Hennekam RC, Hoovers JM. Aalfs CM, et al. Among authors: hoovers jm. Clin Genet. 1996 Jan;49(1):42-5. doi: 10.1111/j.1399-0004.1996.tb04323.x. Clin Genet. 1996. PMID: 8721571

9

Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?

Aalfs CM, Fantes JA, Wenniger-Prick LJ, Sluijter S, Hennekam RC, van Heyningen V, Hoovers JM. Aalfs CM, et al. Among authors: hoovers jm. Am J Med Genet. 1997 Dec 19;73(3):267-71. doi: 10.1002/(sici)1096-8628(19971219)73:3<267::aid-ajmg7>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9415682

10

Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6.

Groen SE, Drewes JG, de Boer EG, Hoovers JM, Hennekam RC. Groen SE, et al. Among authors: hoovers jm. Am J Med Genet. 1998 Dec 28;80(5):448-53. doi: 10.1002/(sici)1096-8628(19981228)80:5<448::aid-ajmg3>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9880207

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