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Items: 1 to 20 of 23

1.

High resolution comparative genomic hybridisation in clinical cytogenetics.

Kirchhoff M, Rose H, Lundsteen C.

J Med Genet. 2001 Nov;38(11):740-4.

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Intrachromosomal triplication of distal 7p.

Rivera H, Bobadilla L, Rolon A, Kunz J, Crolla JA.

J Med Genet. 1998 Jan;35(1):78-80.

5.

Further delineation of 7p trisomy. Case report and review of literature.

Pallotta R, Dalprà L, Fusilli P, Zuffardi O.

Ann Genet. 1996;39(3):152-8. Review.

PMID:
8839888
6.

Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short arm.

Reish O, Berry SA, Dewald G, King RA.

Am J Med Genet. 1996 Jan 2;61(1):21-5. Review.

PMID:
8741912
7.

An apparent balanced translocation between chromosomes 7 and 13 [t(7;13)(p15;q32)] in a 47,XYY individual.

Verma RS, Giridharan R, Conte RA, Luke S.

Jpn J Hum Genet. 1994 Dec;39(4):451-2. No abstract available.

PMID:
7873761
8.

Partial trisomy 7p in two families resulting from different balanced translocations.

Moore CM, Pfeiffer RA, Craig-Holmes AP, Scott CI Jr, Meisel-Stosiek M.

Clin Genet. 1982 Feb;21(2):112-21. No abstract available.

PMID:
7083611
9.

Two pericentric inversions inv(7)(p15;q32) and inv(9)(p11;q13) in a male with absence of vas deferens.

Petit P, Fryns JP.

Hum Genet. 1983;64(3):303. No abstract available.

PMID:
6885077
10.

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
11.

Partial trisomy for 7p due to maternal balanced translocation.

Ohdo S, Suzumori K, Madokoro H, Sonoda T, Hayakawa K.

Jinrui Idengaku Zasshi. 1983 Dec;28(4):297-300. No abstract available.

PMID:
6678317
12.

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
13.

Chromosome abnormalities in 118 couples with recurrent spontaneous abortions.

Tóth A, Gaál M, Bösze P, László J.

Gynecol Obstet Invest. 1984;18(2):72-7.

PMID:
6479698
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15.

Chromosomal imbalance in the offspring of translocation carriers involving 7p. Further contribution with three cases to the partial trisomy 7p phenotype.

Gabarrón J, Glover G, Jiménez A, Salas P, Pérez-Bryan J, Parra MJ.

Clin Genet. 1988 Mar;33(3):211-9.

PMID:
3359679
16.

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
17.

The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

Lindenbaum RH, Hultén M, McDermott A, Seabright M.

J Med Genet. 1985 Feb;22(1):24-8.

18.

Structural rearrangements in the parents of children with primary trisomy 21.

Couzin DA, Watt JL, Stephen GS.

J Med Genet. 1987 May;24(5):280-2.

20.

A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).

Delicado A, Escribano E, Lopez Pajares I, Diaz de Bustamante A, Carrasco S.

J Med Genet. 1991 Feb;28(2):126-7.

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