Format
Sort by
Items per page

Send to

Choose Destination

Links from Books

Items: 9

1.

20p11 deletion in a female child with panhypopituitarism, cleft lip and palate, dysmorphic facial features, global developmental delay and seizure disorder.

Williams PG, Wetherbee JJ, Rosenfeld JA, Hersh JH.

Am J Med Genet A. 2011 Jan;155A(1):186-91. doi: 10.1002/ajmg.a.33763.

PMID:
21204230
2.

De novo trisomy 20p of paternal origin.

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

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

PMID:
17431912
3.

Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling.

Molina-Gomes D, Nebout V, Daikha-Dahmane F, Vialard F, Ville Y, Selva J.

Prenat Diagn. 2006 Mar;26(3):239-41.

PMID:
16485319
4.

Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism.

Faivre L, Viot G, Prieur M, Turleau C, Gosset P, Romana S, Munnich A, Vekemans M, Cormier-Daire V.

Am J Med Genet. 2000 Apr 10;91(4):273-6.

PMID:
10766982
5.

Maternal UPD 20 in a hyperactive child with severe growth retardation.

Chudoba I, Franke Y, Senger G, Sauerbrei G, Demuth S, Beensen V, Neumann A, Hansmann I, Claussen U.

Eur J Hum Genet. 1999 Jul;7(5):533-40.

6.

"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parents.

Wenger SL, Steele MW, Boone LY, Lenkey SG, Cummins JH, Chen XQ.

Am J Med Genet. 1995 Jan 2;55(1):47-52.

PMID:
7702096
7.

del(20p) with manifestations of arteriohepatic dysplasia.

Byrne JL, Harrod MJ, Friedman JM, Howard-Peebles PN.

Am J Med Genet. 1986 Aug;24(4):673-8.

PMID:
3740100
8.

Alagille syndrome and deletion of 20p.

Anad F, Burn J, Matthews D, Cross I, Davison BC, Mueller R, Sands M, Lillington DM, Eastham E.

J Med Genet. 1990 Dec;27(12):729-37. Review.

9.

Alagille syndrome with de novo del(20) (p11.2).

Teebi AS, Murthy DS, Ismail EA, Redha AA.

Am J Med Genet. 1992 Jan 1;42(1):35-8. Review.

PMID:
1308363

Supplemental Content

Support Center