D P Duckett
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Explore the profile of D P Duckett including associated specialties, affiliations and a list of published articles.
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Articles
24
Citations
110
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Recent Articles
1.
Invasive testing for the karyotyping of mid-trimester intrauterine fetal death (IUFD): a pilot study
Howarth E, Konje J, Healey K, Duckett D, Scudamore I, Taylor D
Prenat Diagn
. 2002 Jul;
22(6):453-5.
PMID: 12116301
Introduction: Aneuploidy remains a common cause of fetal loss after the first trimester. Conventional karyotyping from fetal solid tissues post-delivery unfortunately has a poor success rate particularly where the fetus...
2.
Roper E, Konje J, de Chazal R, Duckett D, Oppenheimer C, Taylor D
Prenat Diagn
. 1999 Oct;
19(9):803-7.
PMID: 10521835
Amniocentesis remains the most common prenatal diagnostic invasive procedure for fetal karyotyping. During counselling prior to this procedure miscarriage rates are often quoted as a single figure. In this review...
3.
Long F, Duckett D, Billam L, Williams D, Crolla J
J Med Genet
. 1998 Jun;
35(5):425-8.
PMID: 9610809
A 4 year old female referred with developmental delay was found to have two de novo abnormal derivatives of chromosome 15, a supernumerary inverted duplicated marker chromosome (inv dup(15)) and...
4.
Wilson L, Leverton K, Oude Luttikhuis M, Oley C, Flint J, Wolstenholme J, et al.
Am J Hum Genet
. 1995 Feb;
56(2):400-7.
PMID: 7847374
We report five patients with a combination of brachymetaphalangia and mental retardation, similar to that observed in Albright hereditary osteodystrophy (AHO). Four patients had cytogenetically visible de novo deletions of...
5.
Plaha D, Linforth G, Duckett D, Scott-Jupp R, Tanner M, Jeffreys A
Biotechniques
. 1993 Apr;
14(4):566-7.
PMID: 8476599
No abstract available.
6.
Duckett D, Porter H, Young I
Ann Genet
. 1992 Jan;
35(2):113-6.
PMID: 1524408
A female fetus with a rare de novo chromosome abnormality involving mosaicism with two cell lines with trisomy 13 and presumptive partial monosomy 13 due to a Robertsonian translocation and...
7.
Taylor G, Braddock D, Robson A, Fergusson W, Duckett D, DSouza S, et al.
Clin Exp Immunol
. 1990 Sep;
81(3):501-6.
PMID: 1975779
Monosomy 21 (M21) is a rare aneuploid condition which in certain cases leads to reduced levels of chromosome 21 gene products. We have prepared an Epstein-Barr virus lymphoblastoid cell-line (LCL)...
8.
Young I, Duckett D
J Neurol Neurosurg Psychiatry
. 1990 May;
53(5):441-2.
PMID: 2351981
No abstract available.
9.
Duckett D, Roberts E, McKeever P, Young I
Prenat Diagn
. 1990 Apr;
10(4):261-4.
PMID: 2367342
A de novo case of 'pure' trisomy 14q21----qter is described which was detected at amniocentesis following an abnormal ultrasound scan of a 25-year-old woman. This is apparently the largest distal...
10.
Dickinson A, Fielder A, Young I, Duckett D
Ophthalmic Paediatr Genet
. 1990 Mar;
11(1):1-6.
PMID: 2348977
Patients with Angelman's syndrome have been reported to have ocular hypopigmentation and a number are now known to have a microdeletion of chromosome 15q 11----13. Detailed ocular examination of eight...