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Results: 1 to 20 of 84

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2.

The DNA sequence and analysis of human chromosome 13.

Dunham A, Matthews LH, Burton J, Ashurst JL, Howe KL, Ashcroft KJ, Beare DM, Burford DC, Hunt SE, Griffiths-Jones S, Jones MC, Keenan SJ, Oliver K, Scott CE, Ainscough R, Almeida JP, Ambrose KD, Andrews DT, Ashwell RI, Babbage AK, Bagguley CL, Bailey J, Bannerjee R, Barlow KF, Bates K, Beasley H, Bird CP, Bray-Allen S, Brown AJ, Brown JY, Burrill W, Carder C, Carter NP, Chapman JC, Clamp ME, Clark SY, Clarke G, Clee CM, Clegg SC, Cobley V, Collins JE, Corby N, Coville GJ, Deloukas P, Dhami P, Dunham I, Dunn M, Earthrowl ME, Ellington AG, Faulkner L, Frankish AG, Frankland J, French L, Garner P, Garnett J, Gilbert JG, Gilson CJ, Ghori J, Grafham DV, Gribble SM, Griffiths C, Hall RE, Hammond S, Harley JL, Hart EA, Heath PD, Howden PJ, Huckle EJ, Hunt PJ, Hunt AR, Johnson C, Johnson D, Kay M, Kimberley AM, King A, Laird GK, Langford CJ, Lawlor S, Leongamornlert DA, Lloyd DM, Lloyd C, Loveland JE, Lovell J, Martin S, Mashreghi-Mohammadi M, McLaren SJ, McMurray A, Milne S, Moore MJ, Nickerson T, Palmer SA, Pearce AV, Peck AI, Pelan S, Phillimore B, Porter KM, Rice CM, Searle S, Sehra HK, Shownkeen R, Skuce CD, Smith M, Steward CA, Sycamore N, Tester J, Thomas DW, Tracey A, Tromans A, Tubby B, Wall M, Wallis JM, West AP, Whitehead SL, Willey DL, Wilming L, Wray PW, Wright MW, Young L, Coulson A, Durbin R, Hubbard T, Sulston JE, Beck S, Bentley DR, Rogers J, Ross MT.

Nature. 2004 Apr 1;428(6982):522-8.

4.

Intracytoplasmic sperm injection in infertile patients with structural chromosome abnormalities.

Testart J, Gautier E, Brami C, Rolet F, Sedbon E, Thebault A.

Hum Reprod. 1996 Dec;11(12):2609-12.

5.

CO-FISH reveals inversions associated with isochromosome formation.

Bailey SM, Goodwin EH, Meyne J, Cornforth MN.

Mutagenesis. 1996 Mar;11(2):139-44.

6.

Molecular studies of translocations and trisomy involving chromosome 13.

Robinson WP, Bernasconi F, Dutly F, Lefort G, Romain DR, Binkert F, Schinzel AA.

Am J Med Genet. 1996 Jan 11;61(2):158-63.

PMID:
8669444
7.

Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13;14) trisomy 14.

Antonarakis SE, Blouin JL, Maher J, Avramopoulos D, Thomas G, Talbot CC Jr.

Am J Hum Genet. 1993 Jun;52(6):1145-52.

8.

The effect of 13;14 Robertsonian translocations on germ-cell differentiation in infertile males.

Johannisson R, Schwinger E, Wolff HH, vom Ende V, Löhrs U.

Cytogenet Cell Genet. 1993;63(3):151-5.

PMID:
8485990
9.
10.

Parental origin of the X chromosome in a patient with a Robertsonian translocation and Turner's syndrome.

Krajinovic M, Ivanovic K, Mestroni L, Diklic V, Nikolis J.

J Med Genet. 1994 Mar;31(3):255-6.

11.
12.

Use of the primed in situ labelling (PRINS) technique for a rapid detection of chromosomes 13, 16, 18, 21, X and Y.

Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP.

Hum Genet. 1995 Jan;95(1):12-7.

PMID:
7814017
13.

Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q).

Stallard R, Krueger S, James RS, Schwartz S.

Am J Med Genet. 1995 May 22;57(1):14-8.

PMID:
7645591
14.

13/14 Translocation in a man with reproductive failure. Mitotic and meiotic studies.

Mićić MD, Nikolis JG, Mićić SR.

Hum Genet. 1980;55(1):137-9.

PMID:
7450751
15.

rDNA levels in infertile male carriers of Robertsonian translocations.

Guanti G, Zuffardi O, Tiepolo L.

Cytogenet Cell Genet. 1980;27(2-3):162-7. No abstract available.

PMID:
7398371
16.

Two Robertsonian translocations in a boy with mental retardation.

Lieber E, Shah P.

J Med Genet. 1982 Jun;19(3):229-32. No abstract available.

18.

Dicentric chromosome 13 and centromere inactivation.

Schwartz S, Palmer CG, Weaver DD, Priest J.

Hum Genet. 1983;63(4):332-7.

PMID:
6862437
19.

Two adult siblings with thrombocytopenia and a familial 13;14 translocation.

Nowell P, Besa E, Emanuel B, Pathak S, Finan J.

Cancer Genet Cytogenet. 1984 Feb;11(2):169-74.

PMID:
6692337
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