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Items: 1 to 20 of 82

1.

Editor's comments.

Meadow W.

Acta Paediatr. 2013 Dec;102(12):1129. doi: 10.1111/apa.12415. No abstract available.

PMID:
25132431
2.

More than a diagnosis.

Thiele P, Berg SF, Farlow B.

Acta Paediatr. 2013 Dec;102(12):1127-9. doi: 10.1111/apa.12411. No abstract available.

PMID:
24102789
3.

[Trisomy 13 syndrome (Patau syndrome), trisomy 18 syndrome (Edwards syndrome), Down syndrome (trisomy 21 syndrome), Turner syndrome (XO gonadal dysgenesis)].

Harada N, Niikawa N.

Ryoikibetsu Shokogun Shirizu. 1996;(15):198-201. Review. Japanese. No abstract available.

PMID:
9047985
4.

Trisomy 13 and 18 and quality of life: treading "softly".

Fenton LJ.

Am J Med Genet A. 2011 Jul;155A(7):1527-8. doi: 10.1002/ajmg.a.34084. No abstract available.

PMID:
21671397
5.

Does medical intervention affect outcome in infants with trisomy 18 or trisomy 13?

Kosho T, Carey JC.

Am J Med Genet A. 2016 Apr;170A(4):847-9. doi: 10.1002/ajmg.a.37610. No abstract available.

PMID:
26955783
6.

Medical interventions for children with trisomy 13 and trisomy 18: what is the value of a short disabled life?

Janvier A, Watkins A.

Acta Paediatr. 2013 Dec;102(12):1112-7. doi: 10.1111/apa.12424.

PMID:
24112219
7.

[Should we offer caesarean sections in trisomy 13 and 18?].

Fredheim OM, Hansen TW, Haugen G, Magelssen M.

Tidsskr Nor Laegeforen. 2016 Apr 19;136(7):630-2. doi: 10.4045/tidsskr.15.0037. Norwegian. No abstract available.

8.

Sonographic detection of fetuses with trisomies 13 and 18: accuracy and limitations.

Benacerraf BR, Miller WA, Frigoletto FD Jr.

Am J Obstet Gynecol. 1988 Feb;158(2):404-9.

PMID:
3277433
9.

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

Antonarakis SE, Blouin JL, Maher J, Avramopoulos D, Thomas G, Talbot CC Jr.

Am J Hum Genet. 1993 Jun;52(6):1145-52.

10.
11.

Earlier screening for life-threatening conditions in babies.

[No authors listed]

Community Pract. 2014 Oct;87(10):5. No abstract available.

PMID:
25619056
12.

Chromosomal abnormalities: trisomy 18, trisomy 13, deletions, and microdeletions.

Matthews AL.

J Perinat Neonatal Nurs. 1999 Sep;13(2):59-75; quiz 103-4. Review.

PMID:
10818854
13.
14.

Perinatal care and outcome of fetuses with trisomies 13 and 18 following a parental decision not to terminate the pregnancy.

Sibiude J, Gavard L, Floch-Tudal C, Mandelbrot L.

Fetal Diagn Ther. 2011;29(3):233-7. doi: 10.1159/000322133.

PMID:
21335934
15.

Changes in fetal prevalence and outcome for trisomies 13 and 18: a population-based study over 23 years.

Irving C, Richmond S, Wren C, Longster C, Embleton ND.

J Matern Fetal Neonatal Med. 2011 Jan;24(1):137-41. doi: 10.3109/14767051003758879.

PMID:
20384468
16.

Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.

Porreco RP, Garite TJ, Maurel K, Marusiak B; Obstetrix Collaborative Research Network., Ehrich M, van den Boom D, Deciu C, Bombard A.

Am J Obstet Gynecol. 2014 Oct;211(4):365.e1-12. doi: 10.1016/j.ajog.2014.03.042.

PMID:
24657131
17.

Chromosome abnormalities in selected newborn infants with malformations in Brazil.

Borovik CL, Brunoni D, Sato AE, Barletta H, Dualibi-Casanova L, Hironaka HC, Brunoni LR, Brock R, Carvalho LA, Costa Ede C.

Am J Med Genet. 1989 Nov;34(3):320-4.

PMID:
2596521
18.

Rapid prenatal diagnosis by AmnioPCR and AmnioFISH: routine testing for Down's syndrome (trisomy 21) and sex chromosome trisomies, but targeted testing for Edward's (trisomy 18) and Patau's syndromes (trisomy 13).

Su LL, Biswas A, Ho SS, Ponnusamy S, Kothandaraman N, Chia D, Choolani M.

Ann Acad Med Singapore. 2004 Sep;33(5 Suppl):S53-4. No abstract available.

PMID:
15651208
19.

Developmental status of 22 children with trisomy 18 and eight children with trisomy 13: implications and recommendations.

Bruns DA.

Am J Med Genet A. 2015 Aug;167A(8):1807-15. doi: 10.1002/ajmg.a.37102.

PMID:
25847310
20.

Anodontia totalis fetalis in a trisomy 13 mosaic.

Sperber GH, Honore LH.

J Dent Assoc S Afr. 1988 Nov;43(11):543-6. No abstract available.

PMID:
3272969

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