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Items: 14

1.

Prenatal detection of rare chromosomal autosomal abnormalities in Europe.

Baena N, De Vigan C, Cariati E, Clementi M, Stoll C, Caballin MR, Guitart M; EUROSCAN Working Group..

Am J Med Genet A. 2003 May 1;118A(4):319-27.

PMID:
12687662
2.

Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation.

McCormack WM Jr, Shen JJ, Curry SM, Berend SA, Kashork C, Pinar H, Potocki L, Bejjani BA.

Am J Med Genet. 2002 Nov 1;112(4):384-9. Corrected and republished in: Am J Med Genet A. 2003 Apr 15;118A(2):384-9.

PMID:
12376941
3.

Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme.

Sheridan E, Williams J, Caine A, Morgan R, Mason G, Mueller RF.

Br J Obstet Gynaecol. 1997 Jan;104(1):42-5.

PMID:
8988695
4.

Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus.

Chen CP, Liu FF, Jan SW, Wang KG, Lan CC.

Prenat Diagn. 1996 Jul;16(7):664-6.

PMID:
8843478
5.

Partial trisomy 13 (q21.3 leads to qter) resulting from a maternal translocation t (13;21).

Pangalos C, Couturier J.

Ann Genet. 1981;24(3):179-81. No abstract available.

PMID:
6974532
6.
7.

Deletion of band 13q21 is compatible with normal phenotype.

Couturier J, Morichon-Delvallez N, Dutrillaux B.

Hum Genet. 1985;70(1):87-91.

PMID:
3997156
8.

Chromosome studies of 500 couples with two or more abortions.

Sachs ES, Jahoda MG, Van Hemel JO, Hoogeboom AJ, Sandkuyl LA.

Obstet Gynecol. 1985 Mar;65(3):375-8.

PMID:
3974963
9.

Chromosome studies of males in an institution for the mentally handicapped.

English CJ, Davison EV, Bhate MS, Barrett L.

J Med Genet. 1989 Jun;26(6):379-81.

10.

Deletion long arm 13.

Nielsen J, Homma A, Christiansen F, Rasmussen K, Saldaña-Garcia P.

Hum Genet. 1977 Jul 26;37(3):339-45. No abstract available.

PMID:
885554
11.

Partial deletion of the long arm of chromosome no. 13.

Cuschieri A, Agius PV, Scheres JM.

Hum Genet. 1977 May 10;36(3):341-4.

PMID:
852876
12.

Interstitial deletion 13q syndromes: a report on two unrelated patients.

Serena-Lungarotti M, Calabro A, Mariotti G, Mastroiacovo PP, Provenzano S, Dallapiccola B.

Hum Genet. 1979;52(3):269-74.

PMID:
535887
13.

Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.

Pai GS, Thomas GH, Leonard CO, Ward JC, Valle DL, Pyeritz RE.

Johns Hopkins Med J. 1979 Oct;145(4):162-9. No abstract available.

PMID:
491337
14.

[Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].

de Grouchy J, Turleau C, Danis F, Kohout G, Briard ML.

Ann Genet. 1978 Dec;21(4):247-51. French.

PMID:
314266

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