Mollevanger P - Search Results

1

Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.

Kant SG, Van Haeringen A, Bakker E, Stec I, Donnai D, Mollevanger P, Beverstock GC, Lindeman-Kusse MC, Van Ommen GJ. Kant SG, et al. Among authors: mollevanger p. J Med Genet. 1997 Jul;34(7):569-72. doi: 10.1136/jmg.34.7.569. J Med Genet. 1997. PMID: 9222965 Free PMC article.

2

A girl with 71,XXXXY karyotype.

Maaswinkel-Mooij PD, van Zwieten P, Mollevanger P, van Noort E, Beverstock G. Maaswinkel-Mooij PD, et al. Among authors: mollevanger p. Clin Genet. 1992 Feb;41(2):96-9. doi: 10.1111/j.1399-0004.1992.tb03641.x. Clin Genet. 1992. PMID: 1544219

3

Multiple supernumerary ring chromosomes of different origin in a patient: a clinical report and review of the literature.

Beverstock GC, Bezrookove V, Mollevanger P, van de Kamp JJ, Pearson P, Kouwenberg JM, Rosenberg C. Beverstock GC, et al. Among authors: mollevanger p. Am J Med Genet A. 2003 Oct 1;122A(2):168-73. doi: 10.1002/ajmg.a.20163. Am J Med Genet A. 2003. PMID: 12955771 Review.

4

Premature menopause because of an inherited deletion in the long arm of the X-chromosome.

Veneman TF, Beverstock GC, Exalto N, Mollevanger P. Veneman TF, et al. Among authors: mollevanger p. Fertil Steril. 1991 Mar;55(3):631-3. doi: 10.1016/s0015-0282(16)54199-5. Fertil Steril. 1991. PMID: 2001764 Free article.

5

Trisomy 13 and myelodysplastic syndrome.

Beverstock GC, Ploem JE, Wessels H, van de Keur D, Mollevanger P. Beverstock GC, et al. Among authors: mollevanger p. Cancer Genet Cytogenet. 1990 Sep;48(2):179-82. doi: 10.1016/0165-4608(90)90117-s. Cancer Genet Cytogenet. 1990. PMID: 2397449

6

A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia.

Beverstock GC, de Meijer PH, ten Bokkel Huinink D, Pruijt JF, den Ottolander GJ, Wessels HW, Mollevanger P. Beverstock GC, et al. Among authors: mollevanger p. Cancer Genet Cytogenet. 1996 Jul 15;89(2):132-5. doi: 10.1016/0165-4608(95)00316-9. Cancer Genet Cytogenet. 1996. PMID: 8697419

7

A second case of hexasomy 8 in myelodysplastic syndrome.

Beverstock GC, Wessels HW, Mollevanger P, den Ottolander GJ, Gottlieb DJ. Beverstock GC, et al. Among authors: mollevanger p. Cancer Genet Cytogenet. 1997 Nov;99(1):68-72. doi: 10.1016/s0165-4608(96)00441-4. Cancer Genet Cytogenet. 1997. PMID: 9352798 Review.

8

Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis. A case report and review of the literature.

Beverstock GC, Mollevanger P, Baaij M, Lind J, van Ieperen L, Bartelings MM, Teunissen K, Brandenburg H, Van Opstal D, Los F. Beverstock GC, et al. Among authors: mollevanger p. Cancer Genet Cytogenet. 1999 Nov;115(1):11-8. doi: 10.1016/s0165-4608(99)00084-9. Cancer Genet Cytogenet. 1999. PMID: 10565293 Review.

9

Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library.

Driesen MS, Dauwerse JG, Wapenaar MC, Meershoek EJ, Mollevanger P, Chen KL, Fischbeck KH, van Ommen GJ. Driesen MS, et al. Among authors: mollevanger p. Genomics. 1991 Dec;11(4):1079-87. doi: 10.1016/0888-7543(91)90035-d. Genomics. 1991. PMID: 1783377

10

Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia.

Wessels JW, Mollevanger P, Dauwerse JG, Cluitmans FH, Breuning MH, Beverstock GC. Wessels JW, et al. Among authors: mollevanger p. Blood. 1991 Apr 1;77(7):1555-9. Blood. 1991. PMID: 2009371 Free article.

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