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Results: 11

1.

Temtamy-like syndrome associated with translocation of 2p24 and 9q32.

Talisetti A, Forrester SR, Gregory D, Johnson L, Schneider MC, Kimonis VE.

Clin Dysmorphol. 2003 Jul;12(3):175-7.

PMID:
14564155
[PubMed - indexed for MEDLINE]
2.

Microdissection of chromosome 2--between-arm intrachromosomal insertion.

Friedrich U, Houman M, Sandgaard J, Rosgaard A, Sunde L.

Eur J Hum Genet. 2000 May;8(5):393-5.

PMID:
10854102
[PubMed - indexed for MEDLINE]
Free Article
3.

A case of insertional translocation involving chromosomes 2 and 4.

Asamoah A, Nandi KN, Prouty L, Thurmon TF, Chen H.

Clin Genet. 1998 Feb;53(2):142-6.

PMID:
9611076
[PubMed - indexed for MEDLINE]
4.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Hsu LY, Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH.

Prenat Diagn. 1996 Jan;16(1):1-28.

PMID:
8821848
[PubMed - indexed for MEDLINE]
5.

Paracentric inversions in humans: a review of 446 paracentric inversions with presentation of 120 new cases.

Pettenati MJ, Rao PN, Phelan MC, Grass F, Rao KW, Cosper P, Carroll AJ, Elder F, Smith JL, Higgins MD, et al.

Am J Med Genet. 1995 Jan 16;55(2):171-87. Review.

PMID:
7717416
[PubMed - indexed for MEDLINE]
6.

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses.

Boué A, Gallano P.

Prenat Diagn. 1984 Spring;4 Spec No:45-67.

PMID:
6463033
[PubMed - indexed for MEDLINE]
7.

The value of chromosome analysis in cases of neural tube defects: a case of anencephaly associated with fetal dup(2)(p24----pter).

Singer N, Gersen S, Warburton D.

Prenat Diagn. 1987 Oct;7(8):567-71.

PMID:
3317387
[PubMed - indexed for MEDLINE]
8.

Common fragile sites induced by folate deprivation, BrdU and aphidicolin: their frequency and distribution in Japanese individuals.

Kuwano A, Sugio Y, Murano I, Kajii T.

Jinrui Idengaku Zasshi. 1988 Sep;33(3):355-64. No abstract available.

PMID:
3144619
[PubMed - indexed for MEDLINE]
9.

Human apolipoprotein B: structure of carboxyl-terminal domains, sites of gene expression, and chromosomal localization.

Knott TJ, Rall SC Jr, Innerarity TL, Jacobson SF, Urdea MS, Levy-Wilson B, Powell LM, Pease RJ, Eddy R, Nakai H, et al.

Science. 1985 Oct 4;230(4721):37-43.

PMID:
2994225
[PubMed - indexed for MEDLINE]
10.

An apparent de novo terminal deletion of chromosome 2 (pter----p24:).

Francis GL, Flannery DB, Byrd JR, Fisher ST.

J Med Genet. 1990 Feb;27(2):137-8. No abstract available.

PMID:
2319584
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation.

Mattei MG, Mattei JF, Bernard R, Giraud F.

Hum Genet. 1979 Sep 2;51(1):55-61.

PMID:
500092
[PubMed - indexed for MEDLINE]
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