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Items: 1 to 20 of 29

1.

Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH.

Klein OD, Cotter PD, Moore MW, Zanko A, Gilats M, Epstein CJ, Conte F, Rauen KA.

Clin Genet. 2007 Mar;71(3):260-6.

PMID:
17309649
2.

Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.

Fauth C, Gribble SM, Porter KM, Codina-Pascual M, Ng BL, Kraus J, Uhrig S, Leifheit J, Haaf T, Fiegler H, Carter NP, Speicher MR.

Hum Genet. 2006 Mar;119(1-2):145-53. Epub 2006 Jan 3.

PMID:
16395598
3.
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.
6.

Partial trisomy of chromosome 6q: an interstitial duplication of the long arm.

Zneimer SM, Ziel B, Bachman R.

Am J Med Genet. 1998 Nov 2;80(2):133-5.

PMID:
9805129
7.

Duplication 6q21q23 in two unrelated patients.

Pratt VM, Roberson JR, Weiss L, Van Dyke DL.

Am J Med Genet. 1998 Nov 2;80(2):112-4.

PMID:
9805125
8.

Interstitial deletion of 6q21-q23 associated with split hand.

Tsukahara M, Yoneda J, Azuma R, Nakashima K, Kito N, Ouchi K, Kanehara Y.

Am J Med Genet. 1997 Mar 31;69(3):268-70.

PMID:
9096755
9.

Risk estimates for balanced reciprocal translocation carriers--prenatal diagnosis experience.

Barisić I, Zergollern L, Muzinić D, Hitrec V.

Clin Genet. 1996 Mar;49(3):145-51.

PMID:
8737980
10.

Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter).

Stamberg J, Shapiro J, Valle D, Kuhajda FP, Thomas G, Wissow L.

Clin Genet. 1981 Feb;19(2):122-5.

PMID:
7471508
11.

Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disorders.

Daniel A, Stewart L, Saville T, Brookwell R, Paull H, Purvis-Smith S, Lam-Po-Tang PR.

Am J Med Genet. 1982 Jan;11(1):61-75.

PMID:
7065004
12.

An infant with trisomy 6q21 leads to 6qter.

Neu RL, Gallien JU, Steinberg-Warren N, Wynn RJ, Bannerman RM.

Ann Genet. 1981;24(3):167-9.

PMID:
6974528
13.
14.

Cytogenetic survey in couples with recurrent fetal wastage.

Fryns JP, Kleczkowska A, Kubień E, Petit P, Van den Berghe H.

Hum Genet. 1984;65(4):336-54.

PMID:
6693122
15.
16.

Feasibility of first trimester prenatal diagnosis of Hunter syndrome.

Lykkelund C, Søndergaard F, Therkelsen AJ, Tønnesen T, Rasmussen V, Mikkelsen M, Güttler F, Nyland MH.

Lancet. 1983 Nov 12;2(8359):1147. No abstract available.

PMID:
6138678
17.

Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.

Allderdice PW, Miller OJ, Miller DA, Breg WR, Gendel E, Zelson C.

Humangenetik. 1971;13(3):205-9. No abstract available.

PMID:
5114675
18.

Deletions of the long arm of chromosome 6: two new cases and review of the literature.

Young RS, Fidone GS, Reider-Garcia PA, Hansen KL, McCombs JL, Moore CM.

Am J Med Genet. 1985 Jan;20(1):21-9. Review.

PMID:
3881954
19.

A fetal case of partial trisomy 6q(q21-qter) with renal dysplasia.

Miyabara S, Toyoshima H, Suzumori K.

Jinrui Idengaku Zasshi. 1986 Jun;31(2):93-9. No abstract available.

PMID:
3820772
20.

Cytogenetics of recurrent spontaneous aborters.

McManus SP, de Arce MA.

Ir J Med Sci. 1986 Jul;155(7):216-20. No abstract available.

PMID:
3744746

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