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Items: 1 to 20 of 141

2.

Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q.

Chen CP, Tsai FJ, Lee CC, Chen WL, Pan CW, Wu PC, Wang W.

Genet Couns. 2010;21(3):353-7. No abstract available.

PMID:
20964129
3.

Analysis of a familial 15p + polymorphism: exclusion of Y/15 translocation.

Werner W, Herrmann FH.

Clin Genet. 1984 Sep;26(3):204-8.

PMID:
6478640
4.

Satellited Y chromosomes: structure, origin, and clinical significance.

Schmid M, Haaf T, Solleder E, Schempp W, Leipoldt M, Heilbronner H.

Hum Genet. 1984;67(1):72-85.

PMID:
6745929
5.

Reproductive outcome in 3 families with a satellited chromosome 4 with review of the literature.

Arn PH, Younie L, Russo S, Zackowski JL, Mankinen C, Estabrooks L.

Am J Med Genet. 1995 Jul 3;57(3):420-4. Review.

PMID:
7677144
6.

Ectopic NORs on human chromosomes 4qter and 8q11: rare chromosomal variants detected in two families.

Guttenbach M, Haaf T, Steinlein C, Caesar J, Schinzel A, Schmid M.

J Med Genet. 1999 Apr;36(4):339-42.

7.

Paracentric inversion of chromosome 14 plus rare 9p variant in a couple with habitual spontaneous abortion.

Turczynowicz S, Sharma P, Smith A, Davidson AA.

Ann Genet. 1992;35(1):58-60.

PMID:
1610123
8.

Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes.

Wilkinson TA, Crolla JA.

Hum Genet. 1993 May;91(4):389-91.

PMID:
8500794
9.
10.

[Nucleolus organizer region--centromere translocation].

de Blois MC, Rethoré MO, Lejeune J.

Ann Genet. 1989;32(2):106-8. French.

PMID:
2757357
11.

Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation.

Reddy KS, Murphy T.

Hum Genet. 2000 Sep;107(3):268-75. Review.

PMID:
11071389
12.

A new case of human Y chromosome with satellites on the long arm.

Stella M, Rossi R, Bonfante A, Rossi G.

J Genet Hum. 1980 Mar;28(1):39-45.

PMID:
7190602
13.

A constitutional telomeric translocation showing meiotic instability.

Josifova DJ, Mazzaschi R, Ballard T, Ogilvie CM, Splitt M.

Am J Med Genet A. 2006 Jun 1;140(11):1228-33.

PMID:
16688752
14.

Localization of the nucleolar organizer by computer-aided analysis of a variant no. 21 in a human isolate.

Martin AO, Miller L, Simpson JL, Thomas C, Rzeszotarski MS, Elias S, Sarto GE, Patel VA.

Hum Genet. 1979 Apr 27;48(2):211-9.

PMID:
88411
15.

Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.

Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG.

Eur J Hum Genet. 2007 Apr;15(4):432-40. Epub 2007 Jan 31.

16.

Nonmosaic smallest duplication of 12q24.31-qter: the first reported case.

Ireland JW, Jalal SM, McGrann PS, Lindor NM.

Am J Med Genet A. 2004 Jul 30;128A(3):305-10.

PMID:
15216553
17.

Translocation (Y;22) resulting in the loss of SHOX and isolated short stature.

Borie C, Léger J, Dupuy O, Hassan M, Ledu N, Lebbar A, Czernichow P, Eydoux P.

Am J Med Genet A. 2004 Mar 1;125A(2):186-90.

PMID:
14981722
18.

The effect of variant chromosomes on reproductive fitness in man.

Carothers AD, Buckton KE, Collyer S, De Mey R, Frackiewicz A, Piper J, Smith L.

Clin Genet. 1982 Apr;21(4):280-9.

PMID:
7105475
19.

New insights into the effects of extra nucleolus organizer regions.

Pérez-Castillo A, Martín-Lucas MA, Abrisqueta JA.

Hum Genet. 1986 Jan;72(1):80-2.

PMID:
3455920
20.

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