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Items: 11

1.

Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11.

Tzschach A, Bisgaard AM, Kirchhoff M, Graul-Neumann LM, Neitzel H, Page S, Ahmed A, Müller I, Erdogan F, Ropers HH, Kalscheuer VM, Ullmann R.

Eur J Hum Genet. 2010 Mar;18(3):291-5. doi: 10.1038/ejhg.2009.163. Epub 2009 Oct 21.

2.

Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities.

Balciuniene J, Feng N, Iyadurai K, Hirsch B, Charnas L, Bill BR, Easterday MC, Staaf J, Oseth L, Czapansky-Beilman D, Avramopoulos D, Thomas GH, Borg A, Valle D, Schimmenti LA, Selleck SB.

Am J Hum Genet. 2007 May;80(5):938-47. Epub 2007 Mar 20.

3.

Partial trisomy of chromosome 10(q22-q24) due to maternal insertional translocation (15;10).

Han JY, Kim KH, Jun HJ, Je GH, Glotzbach CD, Shaffer LG.

Am J Med Genet A. 2004 Dec 1;131(2):190-3.

PMID:
15472993
4.

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications.

Kotzot D, Martinez MJ, Bagci G, Basaran S, Baumer A, Binkert F, Brecevic L, Castellan C, Chrzanowska K, Dutly F, Gutkowska A, Karaüzüm SB, Krajewska-Walasek M, Luleci G, Miny P, Riegel M, Schuffenhauer S, Seidel H, Schinzel A.

J Med Genet. 2000 Apr;37(4):281-6.

5.

"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
6.

[Mechanism of duplication formation relating to a case of 10q22 to q25 duplication].

Pison H, Sele B, Salvat J, Pasquier D, Jalbert H, Jalbert P.

Ann Genet. 1982;25(3):137-40. French.

PMID:
6982659
7.
8.

De novo 10q23 interstitial deletion.

Mori MA, Gomez-Sabrido F, Diaz de Bustamante A, Pinel I, Martinez-Frias ML.

J Med Genet. 1988 Mar;25(3):209-10. No abstract available.

10.

[Chromosome aberrations in sterile males. Study of 241 cases].

Bourrouillou G, Colombies P, Blanc P, Grozdea J, Pontonnier F.

Nouv Presse Med. 1978 Nov 25;7(41):3777. French. No abstract available.

PMID:
733534
11.

Familial translocation t(10;21)(q22;q22).

Delicado A, Pajares IL, Vicente P, Hawkins F.

Hum Genet. 1979 Sep;50(3):253-8.

PMID:
489009

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