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Results: 19

1.

An 8.35 Mb overlapping interstitial deletion of 8q24 in two patients with coloboma, congenital heart defect, limb abnormalities, psychomotor retardation and convulsions.

Verheij JB, de Munnik SA, Dijkhuizen T, de Leeuw N, Olde Weghuis D, van den Hoek GJ, Rijlaarsdam RS, Thomasse YE, Dikkers FG, Marcelis CL, van Ravenswaaij-Arts CM.

Eur J Med Genet. 2009 Sep-Oct;52(5):353-7. doi: 10.1016/j.ejmg.2009.05.006. Epub 2009 May 21.

PMID:
19464398
[PubMed - indexed for MEDLINE]
2.

Constitutional t(8;22) in a patient with myasthenia gravis, leukocytosis, and thrombocytosis.

Keung YK, Knovich MA, Molnar I, Pettenati M.

Cancer Genet Cytogenet. 2004 Jan 1;148(1):87-8. No abstract available.

PMID:
14697649
[PubMed - indexed for MEDLINE]
3.

Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.

Wuyts W, Roland D, Lüdecke HJ, Wauters J, Foulon M, Van Hul W, Van Maldergem L.

Am J Med Genet. 2002 Dec 15;113(4):326-32.

PMID:
12457403
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

Incidence of chromosomal rearrangements in couples with reproductive loss.

Kardon NB, Davis JG, Berger AL, Broekman A.

Hum Genet. 1980 Feb;53(2):161-4.

PMID:
7358381
[PubMed - indexed for MEDLINE]
6.

Two human c-onc genes are located on the long arm of chromosome 8.

Neel BG, Jhanwar SC, Chaganti RS, Hayward WS.

Proc Natl Acad Sci U S A. 1982 Dec;79(24):7842-6.

PMID:
6961456
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells.

Dalla-Favera R, Bregni M, Erikson J, Patterson D, Gallo RC, Croce CM.

Proc Natl Acad Sci U S A. 1982 Dec;79(24):7824-7.

PMID:
6961453
[PubMed - indexed for MEDLINE]
Free PMC Article
8.
9.

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
[PubMed - indexed for MEDLINE]
10.

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

Boué A, Gallano P.

Prenat Diagn. 1984 Spring;4 Spec No:45-67.

PMID:
6463033
[PubMed - indexed for MEDLINE]
11.

Partial trisomy 9 in the case of familial translocation 8/9 mat.

Schwanitz G, Schamberger U, Rott HD, Wieczorek V.

Ann Genet. 1974 Sep;17(3):163-6. No abstract available.

PMID:
4548816
[PubMed - indexed for MEDLINE]
12.

A patient with dup(10p)del(8q) and Pendred syndrome.

van Wouwe JP, Wijnands MC, Mourad-Baars PE, Geraedts JP, Beverstock GC, van de Kamp JJ.

Am J Med Genet. 1986 Jun;24(2):211-7.

PMID:
3717206
[PubMed - indexed for MEDLINE]
13.

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.

Daniel A, Hook EB, Wulf G.

Am J Med Genet. 1989 May;33(1):14-53.

PMID:
2750783
[PubMed - indexed for MEDLINE]
15.

Partial trisomy 15q1.

Pfeiffer RA, Kessel E.

Hum Genet. 1976 Jul 7;33(1):77-83.

PMID:
939561
[PubMed - indexed for MEDLINE]
16.

A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat.

Nielsen H, Vetner M, Holm V, Askjaer S, Reske-Nielsen E.

Hum Genet. 1977 Mar 14;35(3):357-62. No abstract available.

PMID:
844879
[PubMed - indexed for MEDLINE]
17.

Familial translocation t(8;14) with a case of tertiary trisomy, +14q-.

Soudek D, Hunter P, O'Shaughnessy S, Simpson NE, Soudek V.

Birth Defects Orig Artic Ser. 1978;14(6C):309-15. No abstract available.

PMID:
728586
[PubMed - indexed for MEDLINE]
18.

[Trisomy 9p - clinical and cytogenetic syndrome].

Hitrec V, Zergollern L.

Acta Med Iugosl. 1979;33(2):169-82. Croatian. No abstract available.

PMID:
506795
[PubMed - indexed for MEDLINE]
19.

Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies.

Frecker M, Dallaire L, Young SR, Chen GC, Simpson NE.

Hum Genet. 1978 Dec 18;45(2):167-73.

PMID:
216625
[PubMed - indexed for MEDLINE]

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