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Related Articles by Review for PubMed (Select 12431252)

1.

Diploid/triploid mosaicism in dysmorphic patients.

van de Laar I, Rabelink G, Hochstenbach R, Tuerlings J, Hoogeboom J, Giltay J.

Clin Genet. 2002 Nov;62(5):376-82. Review.

PMID:
12431252
2.

[Diploid/triploid mosaicism: a variable but characteristic phenotype].

Natera-De Benito D, Poo P, Gean E, Vicente-Villa A, García-Cazorla A, Fons-Estupiña MC.

Rev Neurol. 2014 Aug 16;59(4):158-63. Review. Spanish.

3.

Trisomy 9 mosaicism syndrome. A case report and review of the literature.

Tarani L, Colloridi F, Raguso G, Rizzuti A, Bruni L, Tozzi MC, Palermo D, Panero A, Vignetti P.

Ann Genet. 1994;37(1):14-20. Review.

PMID:
8010707
4.

Diploid/tetraploid mosaicism in a liveborn infant demonstrable only in the bone marrow: case report and literature review.

Aughton DJ, Saal HM, Delach JA, ur Rahman Z, Fisher D.

Clin Genet. 1988 Apr;33(4):299-307. Review.

PMID:
3282728
5.

MCA/MR syndrome in a female infant with tetraploidy mosaicism: review of the human polyploid phenotype.

Wilson GN, Vekemans MJ, Kaplan P.

Am J Med Genet. 1988 Aug;30(4):953-61. Review.

PMID:
3055989
6.

Trisomy 10 mosaicism and maternal uniparental disomy 10 in a liveborn infant with severe congenital malformations.

Hahnemann JM, Nir M, Friberg M, Engel U, Bugge M.

Am J Med Genet A. 2005 Oct 1;138A(2):150-4. Review.

PMID:
16114048
7.

Trisomy 17p10-p12 due to mosaic supernumerary marker chromosome: delineation of molecular breakpoints and clinical phenotype, and comparison to other proximal 17p segmental duplications.

Yatsenko SA, Treadwell-Deering D, Krull K, Lewis RA, Glaze D, Stankiewicz P, Lupski JR, Potocki L.

Am J Med Genet A. 2005 Oct 1;138A(2):175-80. Review.

PMID:
16152635
8.

Congenital anomalies and developmental delay in a boy with double chromosome 6 derived supernumerary marker.

Oldak M, Waligora J, Gieruszczak-Bialek D, Skorka A, Bocian E, Brycz-Witkowska J, Stankiewicz P, Korniszewski L.

Genet Couns. 2006;17(1):29-34. Review.

PMID:
16719274
9.

Diploid/tetraploid mosaicism in a stillborn infant with prune belly anomaly.

Urioste M, Pinel I, Gomar JL, Skinner C, Martinez-Frias ML.

Ann Genet. 1990;33(1):49-51. Review.

PMID:
2195982
10.

[Triploidy syndrome and diploid/triploid mixoploidy syndrome].

Kato R.

Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):361-2. Review. Japanese. No abstract available.

PMID:
11057261
11.

Ocular manifestations of mosaic trisomy 22: a case report and review of the literature.

Thomas S, Parker M, Tan J, Duckett D, Woodruff G.

Ophthalmic Genet. 2004 Mar;25(1):53-6. Review.

PMID:
15255116
12.

Postnatal confirmation of prenatally diagnosed trisomy 20 mosaicism in a patient with linear and whorled nevoid hypermelanosis.

Hartmann A, Hofmann UB, Hoehn H, Broecker EB, Hamm H.

Pediatr Dermatol. 2004 Nov-Dec;21(6):636-41. Review.

PMID:
15575846
13.

[Cohen syndrome. A new case and review of the literature].

Calzolari S, Ballardini M, De Marco P.

Minerva Pediatr. 1995 Mar;47(3):83-7. Review. Italian.

PMID:
7791717
14.

Intrachromosomal triplication for the distal part of chromosome 15q.

Schluth C, Mattei MG, Mignon-Ravix C, Salman S, Alembik Y, Willig J, Ginglinger E, Jeandidier E.

Am J Med Genet A. 2005 Jul 15;136(2):179-84. Review.

PMID:
15940678
15.

Digynic triploid infant surviving for 46 days.

Hasegawa T, Harada N, Ikeda K, Ishii T, Hokuto I, Kasai K, Tanaka M, Fukuzawa R, Niikawa N, Matsuo N.

Am J Med Genet. 1999 Dec 3;87(4):306-10. Review.

PMID:
10588835
16.

Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome.

Callier P, Faivre L, Cusin V, Marle N, Thauvin-Robinet C, Sandre D, Rousseau T, Sagot P, Lacombe E, Faber V, Mugneret F.

Am J Med Genet A. 2005 Aug 30;137(2):204-7. Review.

PMID:
16059936
17.

[Complete triploidy in a live newborn infant. Review and contribution of a new case].

Gillem Lanuza F, Vargas Torcal F, Amelín Chauve MC, Gabarra Lamas J.

An Esp Pediatr. 1988 Aug;29(2):143-8. Review. Spanish.

PMID:
3056149
18.

22q11.2 duplication syndrome: two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes.

Portnoï MF, Lebas F, Gruchy N, Ardalan A, Biran-Mucignat V, Malan V, Finkel L, Roger G, Ducrocq S, Gold F, Taillemite JL, Marlin S.

Am J Med Genet A. 2005 Aug 15;137(1):47-51. Review.

PMID:
16007629
19.

A new neocentromere locus on chromosome 13 resulting in mosaic tetrasomy for distal 13q and an asymmetric phenotype.

Barwell J, Mazzaschi R, Bint S, Ogilvie CM, Elmslie F.

Am J Med Genet A. 2004 Oct 15;130A(3):295-8. Review.

PMID:
15378552
20.

Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.

Gentile M, Volpe P, Cariola F, Di Carlo A, Marotta V, Buonadonna AL, Boscia FM.

Am J Med Genet A. 2005 Jul 1;136(1):66-70. Review.

PMID:
15940687
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