Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Morphology alone does not make an isochromosome.

Literature DB >> 3957349

Morphology alone does not make an isochromosome.

Abstract

Isochromosomes are chromosomes with genetically identical arms. Chromosomes morphologically similar to isochromosomes can arise from alternative mechanisms: whole-arm translocations and crossing over within inversion loops. Cases are presented which could have arisen by each of these latter two mechanisms. The first case is 46,XX,t(15;15) (qter-cen-qter;pter-cen-pter) and the second 46,XY,rec(18),dup q,inv(18) (p11.32q11.2).

Entities: Gene

Mesh：

Year: 1986 PMID： 3957349 DOI： 10.1007/bf00291889

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

16 in total

1. Banding in human chromosomes treated with trypsin.

Authors: H C Wang; S Fedoroff
Journal: Nat New Biol Date: 1972-01-12

2. Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

Authors: H Müller; E M Bühler; E Signer; F Egli; G R Stalder
Journal: J Med Genet Date: 1972-12 Impact factor: 6.318

3. Simultaneous fluorescent staining of R bands and specific heterochromatic regions (DA-DAPI bands) in human chromosomes.

Authors: D Schweizer
Journal: Cytogenet Cell Genet Date: 1980

4. Isochromosome 18q with karyotype 46,XX,i(18q). Cytogenetics and pathology.

Authors: U Froster-Iskenius; W Coerdt; H Rehder; E Schwinger
Journal: Clin Genet Date: 1984-12 Impact factor: 4.438

5. Whole-arm translocation between homologous chromosomes 7 in a woman with successive spontaneous abortions.

Authors: N Niikawa; M Ishikawa
Journal: Hum Genet Date: 1983 Impact factor: 4.132

6. Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism.

Authors: L Y Hsu; S Paciuc; K David; S Cristian; R Moloshok; K Hirschhorn
Journal: J Med Genet Date: 1978-06 Impact factor: 6.318

7. Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.

Authors: L M Larson; W A Wasdahl; J H Saumur; M L Coleman; S M Jalal
Journal: J Med Genet Date: 1978-02 Impact factor: 6.318

8. The Turner phenotype and the different types of human x isochromosome.

Authors: P G Otto; A M Vianna-Morgante; P A Otto; A Wajntal
Journal: Hum Genet Date: 1981 Impact factor: 4.132

Review 9. Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors: M G Mattei; N Souiah; J F Mattei
Journal: Hum Genet Date: 1984 Impact factor: 4.132

10. Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.

Authors: K R Sandig; J Mücke; H Veit
Journal: Hum Genet Date: 1979-11 Impact factor: 4.132

4 in total

1. A molecular genetic approach to the identification of isochromosomes of chromosome 21.

Authors: L G Shaffer; C K Jackson-Cook; J M Meyer; J A Brown; J E Spence
Journal: Hum Genet Date: 1991-02 Impact factor: 4.132

2. Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.

Authors: D F Callen; J C Mulley; E G Baker; G R Sutherland
Journal: Hum Genet Date: 1987-11 Impact factor: 4.132

3. Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

Authors: F A Eggerding; S A Schonberg; F F Chehab; M E Norton; V A Cox; C J Epstein
Journal: Am J Hum Genet Date: 1994-08 Impact factor: 11.025

Review 4. Sibs with tetrasomy 18p born to a mother with trisomy 18p.

Authors: K Takeda; T Okamura; T Hasegawa
Journal: J Med Genet Date: 1989-03 Impact factor: 6.318

4 in total