Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 123

1.

Trisomy 17 in a baboon (Papio hamadryas) with polydactyly, patent foramen ovale and pyelectasis.

Moore CM, Hubbard GB, Dick E, Dunn BG, Raveendran M, Rogers J, Williams V, Gomez JJ, Butler SD, Leland MM, Schlabritz-Loutsevitch NE.

Am J Primatol. 2007 Oct;69(10):1105-18.

PMID:
17330307
2.

Trisomy of chromosome 18 in the baboon (Papio hamadryas anubis).

Howell KH, Hubbard GB, Moore CM, Dunn BG, von Kap-Herr C, Raveendran M, Rogers JA, Leland MM, Brasky KM, Nathanielsz PW, Schlabritz-Loutsevitch NE.

Cytogenet Genome Res. 2006;112(1-2):76-81.

PMID:
16276093
3.

Teratoma with trisomy 16 in a baboon (Papio hamadryas).

Moore CM, McKeand J, Witte SM, Hubbard GB, Rogers J, Leland MM.

Am J Primatol. 1998;46(4):323-32.

PMID:
9839905
4.

Phenotypic variability in Patau syndrome.

Caba L, Rusu C, Butnariu L, Panzaru M, Braha E, Volosciuc M, Popescu R, Gramescu M, Bujoran C, Martiniuc V, Covic M, Gorduza EV.

Rev Med Chir Soc Med Nat Iasi. 2013 Apr-Jun;117(2):321-7.

PMID:
24340511
5.

Partial trisomy 13 with features similar to C syndrome.

Phadke SR, Patil SJ.

Indian Pediatr. 2004 Jun;41(6):614-7.

6.

A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome.

Balci S, Güçer S, Orhan D, Karagöz T.

Turk J Pediatr. 2008 Nov-Dec;50(6):595-9.

PMID:
19227428
7.

Hirschsprung disease, postaxial polydactyly, and atrial septal defect.

Nowaczyk MJ, James AG, Superina R, Siegel-Bartelt J.

Am J Med Genet. 1997 Jan 10;68(1):74-5.

PMID:
8986280
8.

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.

Karadima G, Bugge M, Nicolaidis P, Vassilopoulos D, Avramopoulos D, Grigoriadou M, Albrecht B, Passarge E, Annerén G, Blennow E, Clausen N, Galla-Voumvouraki A, Tsezou A, Kitsiou-Tzeli S, Hahnemann JM, Hertz JM, Houge G, Kuklík M, Macek M, Lacombe D, Miller K, Moncla A, López Pajares I, Patsalis PC, Petersen MB, et al.

Eur J Hum Genet. 1998 Sep-Oct;6(5):432-8.

9.

Unilateral microtia in an infant with trisomy 18 mosaicism.

Giannatou E, Leze H, Katana A, Kolialexi A, Mavrou A, Kanavakis E, Kitsiou-Tzeli S.

Genet Couns. 2009;20(2):181-7.

PMID:
19650416
10.

Parental origin of the extra chromosome 18 in Edwards syndrome.

Ramesh KH, Verma RS.

Ann Genet. 1996;39(2):110-2.

PMID:
8766143
11.

[Trisomy 9p. Report of two new cases].

San Román Muñoz M, Herranz Fernández JL, Tejerina Puente A, Arteaga Manjón-Cabeza R, López Grondona F.

An Pediatr (Barc). 2004 Oct;61(4):336-9. Spanish.

12.

Variable expressivity in Patau syndrome is not all related to trisomy 13 mosaicism.

Hsu HF, Hou JW.

Am J Med Genet A. 2007 Aug 1;143A(15):1739-48.

PMID:
17603803
13.

Impact of trisomy on fertility and meiosis in male mice.

Davisson M, Akeson E, Schmidt C, Harris B, Farley J, Handel MA.

Hum Reprod. 2007 Feb;22(2):468-76. Epub 2006 Oct 17.

PMID:
17050550
14.

De novo trisomy 20p of paternal origin.

Chaabouni M, Turleau C, Karboul L, Jemaa LB, Maazoul F, Attié-Bitach T, Romana S, Chaabouni H.

Am J Med Genet A. 2007 May 15;143A(10):1100-3.

PMID:
17431912
15.

Two cases of trisomy 16 mosaicism ascertained postnatally.

Rieubland C, Francis D, Houben L, Corrie S, Bankier A, White SM.

Am J Med Genet A. 2009 Jul;149A(7):1523-8. doi: 10.1002/ajmg.a.32925.

PMID:
19533780
16.

Pseudotrisomy 13 syndrome in siblings.

Amor DJ, Woods CG.

Clin Dysmorphol. 2000 Apr;9(2):115-8.

PMID:
10826623
17.

Valvular competent patent foramen ovale in adults.

Schroeckenstein RF, Wasenda GJ, Edwards JE.

Minn Med. 1972 Jan;55(1):11-3. No abstract available.

PMID:
5009217
18.

Aplasia and duplication of the thumb and facial clefts associated with fetal trisomy 18.

Chen CP.

Am J Med Genet A. 2006 May 1;140(9):960-3. No abstract available.

PMID:
16575887
19.

Pseudo-trisomy 13 in a fetus: further support for autosomal recessive inheritance.

Utine GE, Alanay Y, Aktaş D, Talim B, Kale G, Tunçbilek E.

Turk J Pediatr. 2008 May-Jun;50(3):287-90.

PMID:
18773678
20.

Maternal origin and clinical findings in a case with trisomy 22.

Mihçi E, Taçoy S, Yakut S, Ongun H, Keser I, Kiliçarslan B, Bağci G, Lüleci G.

Turk J Pediatr. 2007 Jul-Sep;49(3):322-6.

PMID:
17990591

Supplemental Content

Support Center