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Items: 18

1.

Microarray based analysis of 3p25-p26 deletions (3p- syndrome).

Shuib S, McMullan D, Rattenberry E, Barber RM, Rahman F, Zatyka M, Chapman C, Macdonald F, Latif F, Davison V, Maher ER.

Am J Med Genet A. 2009 Oct;149A(10):2099-105. doi: 10.1002/ajmg.a.32824.

PMID:
19760623
2.

Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review.

Malmgren H, Sahlén S, Wide K, Lundvall M, Blennow E.

Am J Med Genet A. 2007 Sep 15;143A(18):2143-9.

PMID:
17696125
3.

Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect.

Takagishi J, Rauen KA, Drumheller T, Kousseff B, Sutcliffe M.

Am J Med Genet A. 2006 Jul 15;140(14):1587-93.

PMID:
16770804
4.

Analysis of CRELD1 as a candidate 3p25 atrioventicular septal defect locus (AVSD2).

Zatyka M, Priestley M, Ladusans EJ, Fryer AE, Mason J, Latif F, Maher ER.

Clin Genet. 2005 Jun;67(6):526-8. No abstract available.

PMID:
15857420
5.

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW.

Am J Hum Genet. 2004 Jun;74(6):1286-93. Epub 2004 Apr 21.

6.

The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation.

Endris V, Wogatzky B, Leimer U, Bartsch D, Zatyka M, Latif F, Maher ER, Tariverdian G, Kirsch S, Karch D, Rappold GA.

Proc Natl Acad Sci U S A. 2002 Sep 3;99(18):11754-9. Epub 2002 Aug 23.

7.

Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.

Cargile CB, Goh DL, Goodman BK, Chen XN, Korenberg JR, Semenza GL, Thomas GH.

Am J Med Genet. 2002 Apr 22;109(2):133-8.

PMID:
11977162
8.

A terminal deletion of the short arm of chromosome 3: karyotype 46, XY, del (3) (p25-pter); a case report and literature review.

Kariya S, Aoji K, Akagi H, Fukushima K, Chikumoto E, Ogawa T, Karaki M, Nishizaki K.

Int J Pediatr Otorhinolaryngol. 2000 Nov 30;56(1):71-8. Review.

PMID:
11074119
9.

Detailed mapping of a congenital heart disease gene in chromosome 3p25.

Green EK, Priestley MD, Waters J, Maliszewska C, Latif F, Maher ER.

J Med Genet. 2000 Aug;37(8):581-7.

10.

CALL gene is haploinsufficient in a 3p- syndrome patient.

Angeloni D, Lindor NM, Pack S, Latif F, Wei MH, Lerman MI.

Am J Med Genet. 1999 Oct 29;86(5):482-5.

PMID:
10508992
11.

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Drumheller T, McGillivray BC, Behrner D, MacLeod P, McFadden DE, Roberson J, Venditti C, Chorney K, Chorney M, Smith DI.

J Med Genet. 1996 Oct;33(10):842-7.

12.

Clinical and molecular analyses of deletion 3p25-pter syndrome.

Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL.

Am J Med Genet. 1993 Jul 1;46(6):623-9.

PMID:
8103286
13.

Molecular genetic analysis of the 3p- syndrome.

Phipps ME, Latif F, Prowse A, Payne SJ, Dietz-Band J, Leversha M, Affara NA, Moore AT, Tolmie J, Schinzel A, et al.

Hum Mol Genet. 1994 Jun;3(6):903-8.

PMID:
7951234
14.

Terminal deletion of the short arm of chromosome 3, del(3pter-p25): a recognizable syndrome.

Schwyzer U, Binkert F, Caflisch U, Baumgartner B, Schinzel A.

Helv Paediatr Acta. 1987;42(4):309-15.

PMID:
3443553
15.

Two infants with del(3)(p25pter) and a review of previously reported cases.

Ramer JC, Ladda RL, Frankel C.

Am J Med Genet. 1989 May;33(1):108-12. Review.

PMID:
2665488
16.

Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.

Narahara K, Kikkawa K, Murakami M, Hiramoto K, Namba H, Tsuji K, Yokoyama Y, Kimoto H.

Am J Med Genet. 1990 Feb;35(2):269-73. Review.

PMID:
2178418
17.

Infant with del(3) (p25-pter): karyotype-phenotype correlation and review of previously reported cases.

Nienhaus H, Mau U, Zang KD.

Am J Med Genet. 1992 Nov 15;44(5):573-5. Review.

PMID:
1481811
18.

A patient with a partial deletion of the short arm of chromosome 3.

Verjaal M, De Nef MB.

Am J Dis Child. 1978 Jan;132(1):43-5.

PMID:
623063

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