Willatt LR[au] - Search Results

Year	Number of Results
1986	1
1992	1
1998	1
2000	1
2001	2
2006	1
2007	1
2008	1
2009	1
2010	1
2011	1
2024	0

1

Partial trisomy of 2p and neuroblastoma.

Willatt LR, Pearson J, Green AJ. Willatt LR, et al. Am J Med Genet. 2001 Aug 15;102(3):304-5. doi: 10.1002/ajmg.1446. Am J Med Genet. 2001. PMID: 11484212 No abstract available.

2

Testis size and dizygotic twins.

Willatt LR, Bartlett DJ. Willatt LR, et al. Nature. 1986 Jun 12-18;321(6071):658. doi: 10.1038/321658a0. Nature. 1986. PMID: 3713850 No abstract available.

3

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.

Tyreman M, Abbott KM, Willatt LR, Nash R, Lees C, Whittaker J, Simonic I. Tyreman M, et al. Among authors: willatt lr. J Med Genet. 2009 Aug;46(8):531-41. doi: 10.1136/jmg.2008.065482. Epub 2009 May 17. J Med Genet. 2009. PMID: 19451135

4

Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Barber JC, Joyce CA, Collinson MN, Nicholson JC, Willatt LR, Dyson HM, Bateman MS, Green AJ, Yates JR, Dennis NR. Barber JC, et al. Among authors: willatt lr. J Med Genet. 1998 Jun;35(6):491-6. doi: 10.1136/jmg.35.6.491. J Med Genet. 1998. PMID: 9643291 Free PMC article.

5

X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.

Kent L, Emerton J, Bhadravathi V, Weisblatt E, Pasco G, Willatt LR, McMahon R, Yates JR. Kent L, et al. Among authors: willatt lr. J Med Genet. 2008 Aug;45(8):519-24. doi: 10.1136/jmg.2008.057729. Epub 2008 Apr 15. J Med Genet. 2008. PMID: 18413370

6

Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.

Willatt LR, Barber JC, Clarkson A, Simonic I, Raymond FL, Docherty Z, Ogilvie CM. Willatt LR, et al. Eur J Hum Genet. 2007 Jan;15(1):45-52. doi: 10.1038/sj.ejhg.5201720. Epub 2006 Sep 20. Eur J Hum Genet. 2007. PMID: 16985501

7

Ring chromosome 12 with inverted microduplication of 12p13.3 involving the Von Willebrand Factor gene associated with cryptogenic stroke in a young adult male.

Nik-Zainal S, Cotter PE, Willatt LR, Abbott K, O'Brien EW. Nik-Zainal S, et al. Among authors: willatt lr. Eur J Med Genet. 2011 Jan-Feb;54(1):97-101. doi: 10.1016/j.ejmg.2010.09.014. Epub 2010 Oct 8. Eur J Med Genet. 2011. PMID: 20933620

8

A case of ring chromosome 2 with growth retardation, mild dysmorphism, and microdeletion of 2p detected using FISH.

Dee SL, Clark AT, Willatt LR, Yates JR. Dee SL, et al. Among authors: willatt lr. J Med Genet. 2001 Sep;38(9):E32. doi: 10.1136/jmg.38.9.e32. J Med Genet. 2001. PMID: 11546833 Free PMC article. No abstract available.

9

A male with trisomy 9 mosaicism and maternal uniparental disomy for chromosome 9 in the euploid cell line.

Willatt LR, Davison BC, Goudie D, Alexander J, Dyson HM, Jenks PE, Ferguson-Smith ME. Willatt LR, et al. J Med Genet. 1992 Oct;29(10):742-4. doi: 10.1136/jmg.29.10.742. J Med Genet. 1992. PMID: 1433238 Free PMC article.

10

Léri-Weill syndrome associated with a pseudodicentric X;Y translocation chromosome and skewed X-inactivation: implications for genetic counselling.

Baralle D, Willatt LR, Shears DJ. Baralle D, et al. Among authors: willatt lr. Am J Med Genet. 2000 Dec 11;95(4):391-5. Am J Med Genet. 2000. PMID: 11186896

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