de Pater JM - Search Results

1

First trimester nuchal anomalies as a prenatal sign of Zellweger syndrome.

Christiaens GC, de Pater JM, Stoutenbeek P, Drogtrop A, Wanders RJ, Beemer FA. Christiaens GC, et al. Among authors: de pater jm. Prenat Diagn. 2000 Jun;20(6):520-1. Prenat Diagn. 2000. PMID: 10861722 No abstract available.

2

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques.

de Pater JM, Govaerts LC, de Man SA, van der Sijs-Bos CJ, Christiaens GC, van Dam WM, Loneus WH, Engelen JJ. de Pater JM, et al. Prenat Diagn. 2003 Sep;23(9):747-51. doi: 10.1002/pd.653. Prenat Diagn. 2003. PMID: 12975787

3

Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22.

de Pater JM, Schuring-Blom GH, van den Bogaard R, van der Sijs-Bos CJ, Christiaens GC, Stoutenbeek P, Leschot NJ. de Pater JM, et al. Prenat Diagn. 1997 Jan;17(1):81-6. doi: 10.1002/(sici)1097-0223(199701)17:1<81::aid-pd29>3.0.co;2-v. Prenat Diagn. 1997. PMID: 9021833

4

Prenatal and postnatal investigation of a case with Miller-Dieker syndrome due to a familial cryptic translocation t(17;20) (p13.3;q13.3) detected by fluorescence in situ hybridization.

van Zelderen-Bhola SL, Breslau-Siderius EJ, Beverstock GC, Stolte-Dijkstra I, de Vries LS, Stoutenbeek P, de Pater JM. van Zelderen-Bhola SL, et al. Among authors: de pater jm, de vries ls. Prenat Diagn. 1997 Feb;17(2):173-9. doi: 10.1002/(sici)1097-0223(199702)17:2<173::aid-pd30>3.0.co;2-v. Prenat Diagn. 1997. PMID: 9061768

5

Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12).

de Pater JM, Scheres JM, Christiaens GC, Ausems MG. de Pater JM, et al. Prenat Diagn. 2003 Jan;23(1):65-7. doi: 10.1002/pd.514. Prenat Diagn. 2003. PMID: 12533816

6

Trisomy 8 in chorionic villi-unpredictable results in follow-up.

de Pater JM, Schuring-Blom GH, Nieste-Otter MA, van Nesselrooij B, Kapitein B, Christiaens GC, Leschot NJ. de Pater JM, et al. Prenat Diagn. 2000 May;20(5):435-7. doi: 10.1002/(sici)1097-0223(200005)20:5<435::aid-pd823>3.0.co;2-q. Prenat Diagn. 2000. PMID: 10820417 No abstract available.

7

[Maternal serum screening for Down syndrome and neural tube defects].

van Rijn M, Christiaens GC, van der Schouw YT, Hagenaars AM, de Pater JM, Visser GH. van Rijn M, et al. Among authors: de pater jm. Ned Tijdschr Geneeskd. 1998 Feb 21;142(8):409-15. Ned Tijdschr Geneeskd. 1998. PMID: 9562776 Dutch.

8

Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes.

Beemer FA, Veenema H, de Pater JM. Beemer FA, et al. Among authors: de pater jm. Am J Med Genet. 1986 Jan-Feb;23(1-2):221-6. doi: 10.1002/ajmg.1320230117. Am J Med Genet. 1986. PMID: 3953650

9

Isochromosome 1q as the sole chromosomal abnormality in two fetal teratomas. Possible trisomic or tetrasomic zygote rescue in fetal teratoma with an additional isochromosome 1q.

Scheres JM, de Pater JM, Stoutenbeek P, Wijmenga C, Rosenberg C, Pearson PL. Scheres JM, et al. Among authors: de pater jm. Cancer Genet Cytogenet. 1999 Nov;115(1):1-10. doi: 10.1016/s0165-4608(99)00049-7. Cancer Genet Cytogenet. 1999. PMID: 10565292

10

Comparative genomic hybridization for cytogenetic evaluation of stillbirth.

Christiaens GC, Vissers J, Poddighe PJ, de Pater JM. Christiaens GC, et al. Among authors: de pater jm. Obstet Gynecol. 2000 Aug;96(2):281-6. doi: 10.1016/s0029-7844(00)00879-6. Obstet Gynecol. 2000. PMID: 10908778

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

35 results

Search Page

Filters