Hamers G - Search Results

1

Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis.

Van Opstal D, Boter M, Noomen P, Srebniak M, Hamers G, Galjaard RJ. Van Opstal D, et al. Among authors: hamers g. Mol Cytogenet. 2011 Jan 14;4:2. doi: 10.1186/1755-8166-4-2. Mol Cytogenet. 2011. PMID: 21235775 Free PMC article.

2

Prenatal diagnosis of trisomy 12 mosaicism: normal development of a 3 years old female child.

Staals JE, Schrander-Stumpel CT, Hamers G, Fryns JP. Staals JE, et al. Among authors: hamers g. Genet Couns. 2003;14(2):233-7. Genet Couns. 2003. PMID: 12872819 Review.

3

Marker chromosome identification by micro-FISH.

Engelen JJ, Loots WJ, Motoh PC, Moog U, Hamers GJ, Geraedts JP. Engelen JJ, et al. Among authors: hamers gj. Clin Genet. 1996 May;49(5):242-8. doi: 10.1111/j.1399-0004.1996.tb03781.x. Clin Genet. 1996. PMID: 8832132

4

Translocation t(2;3)(p15-23;q26-27) in myeloid malignancies: report of 21 new cases, clinical, cytogenetic and molecular genetic features.

Stevens-Kroef M, Poppe B, van Zelderen-Bhola S, van den Berg E, van der Blij-Philipsen M, Geurts van Kessel A, Slater R, Hamers G, Michaux L, Speleman F, Hagemeijer A. Stevens-Kroef M, et al. Among authors: hamers g. Leukemia. 2004 Jun;18(6):1108-14. doi: 10.1038/sj.leu.2403346. Leukemia. 2004. PMID: 15085164

5

Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature.

Schrander-Stumpel C, Schrander J, Fryns JP, Hamers G. Schrander-Stumpel C, et al. Among authors: hamers g. Clin Genet. 1990 Feb;37(2):148-52. doi: 10.1111/j.1399-0004.1990.tb03492.x. Clin Genet. 1990. PMID: 2178819 Review.

6

The partial monosomy 10q syndrome: report on two patients and review of the developmental data.

Schrander-Stumpel C, Fryns JP, Hamers G. Schrander-Stumpel C, et al. Among authors: hamers g. J Ment Defic Res. 1991 Jun;35 ( Pt 3):259-67. doi: 10.1111/j.1365-2788.1991.tb01059.x. J Ment Defic Res. 1991. PMID: 1920392 Review.

7

Caudal deficiency sequence in 7q terminal deletion.

Schrander-Stumpel C, Schrander J, Fryns JP, Hamers G. Schrander-Stumpel C, et al. Among authors: hamers g. Am J Med Genet. 1988 Jul;30(3):757-61. doi: 10.1002/ajmg.1320300309. Am J Med Genet. 1988. PMID: 3055986 Review.

8

Mosaic trisomy 11p in monozygotic twins with discordant clinical phenotypes.

Marcus-Soekarman D, Hamers G, Velzeboer S, Nijhuis J, Loneus WH, Herbergs J, de Die-Smulders C, Schrander-Stumpel C, Engelen J. Marcus-Soekarman D, et al. Among authors: hamers g. Am J Med Genet A. 2004 Jan 30;124A(3):288-91. doi: 10.1002/ajmg.a.20403. Am J Med Genet A. 2004. PMID: 14708102

9

Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype.

Marcus-Soekarman D, Hamers G, Mulder AL, Offermans J, Offermans J, Engelen J, van Lent-Albrechts JC, Robben SG, de Muinck Keizer-Schrama S, Wolffenbuttel KP, Looijenga LH, Oosterhuis JW, Schrander-Stumpel C, Nijhuis J. Marcus-Soekarman D, et al. Among authors: hamers g. Prenat Diagn. 2005 Apr;25(4):279-82. doi: 10.1002/pd.996. Prenat Diagn. 2005. PMID: 15849784

10

Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution banding.

de Die-Smulders CE, Engelen JJ, Albrechts JC, Hamers GJ. de Die-Smulders CE, et al. Among authors: hamers gj. Am J Med Genet. 1999 Oct 8;86(4):385-8. doi: 10.1002/(sici)1096-8628(19991008)86:4<385::aid-ajmg14>3.0.co;2-s. Am J Med Genet. 1999. PMID: 10494096

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