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
11.
Plaha D, Duckett D, Collacott R, Young I
J Med Genet
. 1990 Mar;
27(3):203-4.
PMID: 1969965
No abstract available.
12.
Collacott R, Duckett D, Mathews D, Warrington J, Young I
J Ment Defic Res
. 1990 Feb;
34 ( Pt 1):81-6.
PMID: 2139133
A profoundly mentally handicapped patient is described with the karyotype 47,X, fra (X) (q27), + 21. Her phenotype demonstrates features of both Down's Syndrome and fragile-X syndrome. The authors believe...
13.
Young I, Duckett D, OReilly K
Ann Genet
. 1989 Jan;
32(1):62-4.
PMID: 2751252
A lethally malformed neonate with mosaic tetrasomy 12p is presented. This is the third reported case of mosaic tetrasomy 12p to have died in the neonatal period. These three babies...
14.
Dalgleish R, Duckett D, Woodhouse M, Shannon R, Young I
J Med Genet
. 1988 Dec;
25(12):851-4.
PMID: 3236369
A three and a half year old mildly retarded boy is presented. Karyotyping showed monosomy 21 (45,XY,-21) in all 50 metaphase spreads examined from two lymphocyte cultures, and in 20%...
15.
Roberts E, Duckett D, Lang G
Prenat Diagn
. 1988 Nov;
8(9):635-40.
PMID: 3211852
Presumptive maternal cell contamination (MCC) was monitored in identified male cases during cytogenetic comparison of direct techniques and three different culture regimens from 140 thoroughly dissected chorionic villus samples. Of...
16.
Duckett D, Young I
Hum Genet
. 1988 Jul;
79(3):251-4.
PMID: 3042599
A 7 3/4-year-old girl with short stature was found to have a recombinant (X),dup q chromosome resulting from an apparently unique pericentric inversion (X)(p11.2q26) present in her mother and maternal...
17.
Mehta L, Duckett D, Young I
J Med Genet
. 1987 Mar;
24(3):185-6.
PMID: 3573005
No abstract available.
18.
Mehta L, Shannon R, Duckett D, Young I
J Med Genet
. 1986 Jun;
23(3):256-7.
PMID: 3723555
A 13 year old girl with trisomy 18 is described. She showed profound mental and growth retardation, severe kyphoscoliosis, and unusual ocular features including discontinuous eyebrows, distichiasis, and blue sclerae.
19.
Duckett D, Roberts S, Davies P
Hum Genet
. 1984 Jan;
67(2):156-61.
PMID: 6336319
A case of Prader-Willi syndrome (PWS) associated with a de novo unbalanced 15q;17q reciprocal translocation presumptively resulting from the tertiary monosomic form of 3:1 meiotic disjunction is described. Twenty-three similar...
20.
Roberts S, Duckett D, Laurence K
J Med Genet
. 1982 Dec;
19(6):465-7.
PMID: 7154046
No abstract available.