Los FJ - Search Results

1

De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data.

Los FJ, Van Hemel JO, Jacobs HJ, Drop SL, van Dongen JJ. Los FJ, et al. J Med Genet. 1994 Jan;31(1):72-3. doi: 10.1136/jmg.31.1.72. J Med Genet. 1994. PMID: 8151644 Free PMC article.

2

A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei.

van Opstal D, van Hemel JO, Eussen BH, van der Heide A, van den Berg C, In 'T Veld PA, Los FJ. van Opstal D, et al. Among authors: los fj. Prenat Diagn. 1995 Aug;15(8):705-11. doi: 10.1002/pd.1970150805. Prenat Diagn. 1995. PMID: 7479588 Free article.

3

DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63).

van den Ouweland AM, van der Est MN, Wesby-van Swaay E, Tijmensen TS, Los FJ, Van Hemel JO, Hennekam RC, Meijers-Heijboer HJ, Niermeijer MF, Halley DJ. van den Ouweland AM, et al. Among authors: los fj. Hum Genet. 1995 May;95(5):562-7. doi: 10.1007/BF00223870. Hum Genet. 1995. PMID: 7759079

4

Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection.

Van Opstal D, Los FJ, Ramlakhan S, Van Hemel JO, Van Den Ouweland AM, Brandenburg H, Pieters MH, Verhoeff A, Vermeer MC, Dhont M, In't Veld PA. Van Opstal D, et al. Among authors: los fj. Hum Reprod. 1997 Apr;12(4):682-6. doi: 10.1093/humrep/12.4.682. Hum Reprod. 1997. PMID: 9159424 Free article.

5

Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection.

Veld PA, Weber RF, Los FJ, den Hollander N, Dhont M, Pieters MH, Van Hemel JO. Veld PA, et al. Among authors: los fj. Hum Reprod. 1997 Aug;12(8):1642-4. doi: 10.1093/humrep/12.8.1642. Hum Reprod. 1997. PMID: 9308785 Free article.

6

Prenatal cytogenetic and postnatal molecular studies on 46,XX male.

Sachs ES, Van Hemel JO, Los FJ. Sachs ES, et al. Among authors: los fj. Lancet. 1992 Jan 18;339(8786):180-1. doi: 10.1016/0140-6736(92)90245-x. Lancet. 1992. PMID: 1346031 No abstract available.

7

Ring chromosome 18 in a fetus with only facial anomalies.

Los FJ, van den Berg C, Braat PG, Cha'ban FK, Kros JM, Van Opstal D. Los FJ, et al. Am J Med Genet. 1996 Dec 11;66(2):216-20. doi: 10.1002/(SICI)1096-8628(19961211)66:2<216::AID-AJMG18>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8958334

8

[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: los fj. Ned Tijdschr Geneeskd. 1998 Feb 28;142(9):485. Ned Tijdschr Geneeskd. 1998. PMID: 9562765 Dutch. No abstract available.

9

Case of 45,X/46,XY mosaicism with non-mosaic discordance between short-term villi (45,X) and cultured villi (46,XY).

van den Berg C, Van Opstal D, Brandenburg H, Los FJ. van den Berg C, et al. Among authors: los fj. Am J Med Genet. 2000 Jul 31;93(3):230-3. doi: 10.1002/1096-8628(20000731)93:3<230::aid-ajmg14>3.0.co;2-o. Am J Med Genet. 2000. PMID: 10925388

10

Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.

van den Berg C, Pijpers L, Halley DJ, Opstal DV, Los FJ. van den Berg C, et al. Among authors: los fj. Am J Med Genet. 1999 Sep 10;86(2):151-5. Am J Med Genet. 1999. PMID: 10449651

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