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Items: 1 to 20 of 23

1.

A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotype.

Efron D, Delatycki MB, de Silva MG, Langbein A, Slaghuis W, Larson A, Dahl HH, Forrest SM.

J Med Genet. 2003 Feb;40(2):E15. No abstract available.

2.

Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinoma.

Li FP, Decker HJ, Zbar B, Stanton VP Jr, Kovacs G, Seizinger BR, Aburatani H, Sandberg AA, Berg S, Hosoe S, Brown RS.

Ann Intern Med. 1993 Jan 15;118(2):106-11.

PMID:
8416305
3.

Parental chromosome translocations and fetal loss.

Tsenghi C, Metaxotou C, Kalpini-Mavrou A, Strataki-Benetou M, Matsaniotis N.

Obstet Gynecol. 1981 Oct;58(4):456-8.

PMID:
7279340
4.

Balanced rearrangements of the autosomes: results of a longitudinal study of a newborn survey population.

Tierney I, Axworthy D, Smith L, Ratcliffe SG.

J Med Genet. 1984 Feb;21(1):45-51.

5.

Reproductive risks for translocation carriers: cytogenetic study and analysis of pregnancy outcome in 58 families.

Neri G, Serra A, Campana M, Tedeschi B.

Am J Med Genet. 1983 Dec;16(4):535-61.

PMID:
6660248
6.

Inducible fragile site on chromosome 3.

Markkanen A, Knuutila S, de la Chapelle A.

Hum Genet. 1983;65(2):217-8. No abstract available.

PMID:
6654339
7.
8.

Human chromosome hot points. 1. Hot point at 3p14 in three populations.

Zhou XT, Xu BH, Chu CL, Xia GF, Li N, Sha R.

Hum Genet. 1984;67(3):249-51.

PMID:
6469239
9.
10.

Partial trisomy of chromosome 3(p14----p22) due to maternal insertional translocation.

Kleczkowska A, Fryns JP, Van den Berghe H.

Ann Genet. 1984;27(3):180-3. No abstract available.

PMID:
6334484
12.

[De novo t(3 ; 20) (p 14 ; p 12) translocation in a young girl].

Stoll C, Levy JM.

Ann Genet. 1974 Sep;17(3):197-9. French. No abstract available.

PMID:
4548822
13.

[Heterozygosity and homozygosity for a pericentric inversion of human chromosone 3].

Betz A, Turleau C, de Grouchy J.

Ann Genet. 1974 Jun;17(2):79-80. French. No abstract available.

PMID:
4547944
14.

Verification of the previously reported t(3p minus:17q plus) by G banding.

Subrt I.

Humangenetik. 1974;23(3):233-4. No abstract available.

PMID:
4136169
15.

An analysis of the break points of structural rearrangements in man.

Jacobs PA, Buckton KE, Cunningham C, Newton M.

J Med Genet. 1974 Mar;11(1):50-64. No abstract available.

16.

Constitutional del(3)(p14-p21) in a patient with bladder carcinoma.

Barrios L, Miró R, Caballín MR, Vayreda J, Subias A, Egozcue J.

Cancer Genet Cytogenet. 1986 Mar 15;21(2):171-3. No abstract available.

PMID:
3948145
17.
18.

Karyotypes of 1142 couples with recurrent abortion.

Portnoï MF, Joye N, van den Akker J, Morlier G, Taillemite JL.

Obstet Gynecol. 1988 Jul;72(1):31-4.

PMID:
3242501
20.

A population cytogenetic study of a common fragile site, fra(3)(p14), in a healthy population.

Murata M, Otsuka M, Hayakawa Y, Takahashi E, Tsuji H, Hori T.

Jinrui Idengaku Zasshi. 1990 Dec;35(4):291-302.

PMID:
2094778

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