Robinson WP - Search Results

1

Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.

Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G. Wieczorek D, et al. Among authors: robinson wp. Prenat Diagn. 2003 Feb;23(2):128-33. doi: 10.1002/pd.557. Prenat Diagn. 2003. PMID: 12575019

2

Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.

Gillessen-Kaesbach G, Robinson W, Lohmann D, Kaya-Westerloh S, Passarge E, Horsthemke B. Gillessen-Kaesbach G, et al. Hum Genet. 1995 Dec;96(6):638-43. doi: 10.1007/BF00210291. Hum Genet. 1995. PMID: 8522319

3

Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.

Langlois S, Yong PJ, Yong SL, Barrett I, Kalousek DK, Miny P, Exeler R, Morris K, Robinson WP. Langlois S, et al. Among authors: robinson wp. Prenat Diagn. 2006 Jun;26(6):548-58. doi: 10.1002/pd.1457. Prenat Diagn. 2006. PMID: 16683298

4

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.

Dittrich B, Robinson WP, Knoblauch H, Buiting K, Schmidt K, Gillessen-Kaesbach G, Horsthemke B. Dittrich B, et al. Among authors: robinson wp. Hum Genet. 1992 Nov;90(3):313-5. doi: 10.1007/BF00220089. Hum Genet. 1992. PMID: 1487250

5

Prenatally detected trisomy 20 mosaicism.

Robinson WP, McGillivray B, Lewis ME, Arbour L, Barrett I, Kalousek DK. Robinson WP, et al. Prenat Diagn. 2005 Mar;25(3):239-44. doi: 10.1002/pd.1121. Prenat Diagn. 2005. PMID: 15791659

6

Analysis of nine pregnancies with confined placental mosaicism for trisomy 2.

Shaffer LG, Langlois S, McCaskill C, Main DM, Robinson WP, Barrett IJ, Kalousek DK. Shaffer LG, et al. Among authors: robinson wp. Prenat Diagn. 1996 Oct;16(10):899-905. doi: 10.1002/(SICI)1097-0223(199610)16:10<899::AID-PD960>3.0.CO;2-M. Prenat Diagn. 1996. PMID: 8938058

7

The association between preeclampsia and placental trisomy 16 mosaicism.

Yong PJ, Langlois S, von Dadelszen P, Robinson W. Yong PJ, et al. Prenat Diagn. 2006 Oct;26(10):956-61. doi: 10.1002/pd.1534. Prenat Diagn. 2006. PMID: 16874839

8

Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.

Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK. Robinson WP, et al. Prenat Diagn. 2002 Dec;22(12):1076-85. doi: 10.1002/pd.483. Prenat Diagn. 2002. PMID: 12454962

9

Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios.

Hansen WF, Bernard LE, Langlois S, Rao KW, Chescheir NC, Aylsworth AS, Smith DI, Robinson WP, Barrett IJ, Kalousek DK. Hansen WF, et al. Among authors: robinson wp. Prenat Diagn. 1997 May;17(5):443-50. doi: 10.1002/(sici)1097-0223(199705)17:5<443::aid-pd82>3.0.co;2-2. Prenat Diagn. 1997. PMID: 9178319

10

Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy.

Kuchinka BD, Barrett IJ, Moya G, Sánchez JM, Langlois S, Yong SL, Kalousek DK, Robinson WP. Kuchinka BD, et al. Among authors: robinson wp. Prenat Diagn. 2001 Jan;21(1):36-9. doi: 10.1002/1097-0223(200101)21:1<36::aid-pd979>3.0.co;2-1. Prenat Diagn. 2001. PMID: 11180238

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

301 results

Search Page

Filters