Govaerts LC - Search Results

1

Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14).

de Vries BB, Eussen BH, van Diggelen OP, van Der Heide A, Deelen WH, Govaerts LC, Lindhout D, Wouters CH, Van Hemel JO. de Vries BB, et al. Among authors: govaerts lc. Am J Med Genet. 1999 Nov 19;87(2):189-94. doi: 10.1002/(sici)1096-8628(19991119)87:2<189::aid-ajmg12>3.3.co;2-h. Am J Med Genet. 1999. PMID: 10533035

2

Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome.

van Haelst MM, Eussen HJ, Visscher F, de Ruijter JL, Drop SL, Lindhout D, Wouters CH, Govaerts LC. van Haelst MM, et al. Among authors: govaerts lc. J Med Genet. 2002 Aug;39(8):582-5. doi: 10.1136/jmg.39.8.582. J Med Genet. 2002. PMID: 12161598 Free PMC article. No abstract available.

3

Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.

de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP. de Die-Smulders CE, et al. Among authors: govaerts lc. Am J Med Genet. 1995 Nov 20;59(3):369-74. doi: 10.1002/ajmg.1320590318. Am J Med Genet. 1995. PMID: 8599364 Review.

4

Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.

Wouters CH, van Bodegom TM, Moll HA, Govaerts LC. Wouters CH, et al. Among authors: govaerts lc. Ann Genet. 1999;42(3):160-5. Ann Genet. 1999. PMID: 10526659

5

Phenotype-genotype correlation in a familial IGF1R microdeletion case.

Veenma DC, Eussen HJ, Govaerts LC, de Kort SW, Odink RJ, Wouters CH, Hokken-Koelega AC, de Klein A. Veenma DC, et al. Among authors: govaerts lc. J Med Genet. 2010 Jul;47(7):492-8. doi: 10.1136/jmg.2009.070730. Epub 2009 Dec 2. J Med Genet. 2010. PMID: 19955558

6

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

Warburton PE, Dolled M, Mahmood R, Alonso A, Li S, Naritomi K, Tohma T, Nagai T, Hasegawa T, Ohashi H, Govaerts LC, Eussen BH, Van Hemel JO, Lozzio C, Schwartz S, Dowhanick-Morrissette JJ, Spinner NB, Rivera H, Crolla JA, Yu C, Warburton D. Warburton PE, et al. Among authors: govaerts lc. Am J Hum Genet. 2000 Jun;66(6):1794-806. doi: 10.1086/302924. Epub 2000 Apr 24. Am J Hum Genet. 2000. PMID: 10777715 Free PMC article. Review.

7

CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21) (q13.1;q22.3).

De Krijger RR, Mooy CM, Van Hemel JO, Sulkers EJ, Kros JM, Bartelings MM, Govaerts LC. De Krijger RR, et al. Among authors: govaerts lc. Pediatr Dev Pathol. 1999 Nov-Dec;2(6):577-81. doi: 10.1007/s100249900165. Pediatr Dev Pathol. 1999. PMID: 10508883

8

Genetic risk factors in infertile men with severe oligozoospermia and azoospermia.

Dohle GR, Halley DJ, Van Hemel JO, van den Ouwel AM, Pieters MH, Weber RF, Govaerts LC. Dohle GR, et al. Among authors: govaerts lc. Hum Reprod. 2002 Jan;17(1):13-6. doi: 10.1093/humrep/17.1.13. Hum Reprod. 2002. PMID: 11756355 Free article.

9

A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat.

Veltman I, van Asseldonk M, Schepens M, Stoop H, Looijenga L, Wouters C, Govaerts L, Suijkerbuijk R, van Kessel A. Veltman I, et al. Cancer Genet Cytogenet. 2002 Jul 1;136(1):17-22. doi: 10.1016/s0165-4608(01)00666-5. Cancer Genet Cytogenet. 2002. PMID: 12165446

10

[Finishing a pregnancy in an infaust fetal prognosis].

Niermeijer MF, Los FJ, Govaerts LC, van Hemel JO, Wouters CH. Niermeijer MF, et al. Among authors: govaerts lc. Ned Tijdschr Geneeskd. 1998 Feb 28;142(9):485. Ned Tijdschr Geneeskd. 1998. PMID: 9562765 Dutch. No abstract available.

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