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Literature DB >> 4563067

Partial monosomies 18. Review of cytogenetical and phenotypical variants.

I W Lurie, G I Lazjuk.

Abstract

Mesh：

Substances：
Immunoglobulins

Year: 1972 PMID： 4563067 DOI： 10.1007/bf00702354

Source DB: PubMed Journal: Humangenetik ISSN： 0018-7348

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117 in total

1. [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].

Authors: J DE GROUCHY; P ROYER; C SALMON; M LAMY
Journal: Pathol Biol Date: 1964-05

2. Structural variation in human nitotic chromosomes.

Authors: J Leisti
Journal: Ann Acad Sci Fenn Biol Date: 1971

Review 3. Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors: E Passarge
Journal: Humangenetik Date: 1970

4. [A recent case of partial deletion of short arm of chromosome 18].

Authors: J C Vaillaud; J Martin; N Ayraud
Journal: Ann Genet Date: 1970-06

5. [Short-arm deletion of chromosome 18 due to a t(G-;18p+) translocation. Fluorescence study with quinacrine mustard].

Authors: G Malpuech; E J Raynaud; J Belin; P Godeneche; J de Grouchy
Journal: Ann Genet Date: 1971-09

6. Familial 18 q- syndrome.

Authors: E M Law; J G Masterson
Journal: Ann Genet Date: 1969-12

7. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].

Authors: S Gilgenkrantz; C Marchal; N Neimann
Journal: Ann Genet Date: 1968-03

8. [Double and single aneuploidy 48-E+, XXX-47-E+, XX in Edward's syndrome].

Authors: H Waller; M Waller; W Weigel
Journal: Dtsch Gesundheitsw Date: 1969-06-19

9. Clinical and chromosomal studies of the 18q- syndrome.

Authors: W Wertelecki; P S Gerald
Journal: J Pediatr Date: 1971-01 Impact factor: 4.406

10. Ring chromosome 18 in a patient with multiple anomalies.

Authors: C G Palmer; N Fareed; A D Merritt
Journal: J Med Genet Date: 1967-06 Impact factor: 6.318

13 in total

1. Further studies on the genetic heterogeneity of cebocephaly.

Authors: G I Lazjuk; I W Lurie; M K Nedzved
Journal: J Med Genet Date: 1976-08 Impact factor: 6.318

Review 2. Genetics of the +p9 syndrome.

Authors: I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal: Hum Genet Date: 1976-04-15 Impact factor: 4.132

Review 3. Heart disease associated with deletion of the short arm of chromosome 18.

Authors: W Pearl
Journal: Pediatr Cardiol Date: 1989 Impact factor: 1.655

4. Identification of a 18-21 translocation with Klinefelter's syndrome by G-band patterns.

Authors: C Waldenmaier; W Hirsch; E König; K Shibata
Journal: Humangenetik Date: 1974-03-28

5. Letter: Turner's, Ullrich's, and Noonan's syndromes.

Authors: P E Polani
Journal: Br Med J Date: 1974-04-20

6. 18p--syndrome resulting from translocation (13a;18q) in a mildly affected adult male.

Authors: S J Moedjono; S J Funderburk; R S Sparkes
Journal: J Med Genet Date: 1979-10 Impact factor: 6.318

7. Familial mental retardation in a family with an inherited chromosome rearrangement.

Authors: A E Chudley; F Bauder; M Ray; P J McAlpine; S D Pena; J L Hamerton
Journal: J Med Genet Date: 1974-12 Impact factor: 6.318

8. 18p-Mosaicism: case report and review.

Authors: T Motegi; A Ichikawa; M Noda; G Hashimoto; M Kaga
Journal: Hum Genet Date: 1978-10-31 Impact factor: 4.132

9. 18p--syndrome resulting from 14q/18q 'dicentric' fusion translocation.

Authors: S J Funderburk; R S Sparkes; I Klisak
Journal: Hum Genet Date: 1977-11-10 Impact factor: 4.132

10. The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.

Authors: G A Silverman; S S Schneider; H F Massa; A Flint; M Lalande; J C Leonard; J Overhauser; G van den Engh; B J Trask
Journal: Am J Hum Genet Date: 1995-04 Impact factor: 11.025