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Literature DB >> 4133276

Trisomy 13 with a 13-X translocation.

B F Crandall, R E Carrel, J Howard, W A Schroeder, H Müller.

Abstract

Entities: Disease

Mesh：

Substances：
Tritium
Thymidine

Year: 1974 PMID： 4133276 PMCID： PMC1762608

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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18 in total

1. Studies on the induction of translocations in mouse spermatogonia. IV. Effects of acute gamma-irradiation.

Authors: A G Searle; C V Beechey; E P Evans; C E Ford; D G Papworth
Journal: Mutat Res Date: 1971-08 Impact factor: 2.433

2. Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

Authors: T H Thelen; D J Abrams; R O Fisch
Journal: Am J Hum Genet Date: 1971-07 Impact factor: 11.025

3. Studies on the heterogeneity of hemoglobin. 13. Chromatography of various human and animal hemoglobin types on DEAE-Sephadex.

Authors: A M Dozy; E F Kleihauer; T H Huisman
Journal: J Chromatogr Date: 1968-02-20

4. Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.

Authors: A I Taylor
Journal: J Med Genet Date: 1968-09 Impact factor: 6.318

5. An improved method for quantitative determination of human fetal hemoglobin.

Authors: W A Schroeder; T H Huisman; J R Shelton; J B Wilson
Journal: Anal Biochem Date: 1970-05 Impact factor: 3.365

6. Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents.

Authors: T Caspersson; L Zech; C Johansson
Journal: Exp Cell Res Date: 1970-10 Impact factor: 3.905

7. Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins.

Authors: T H Huisman; A M Dozy
Journal: J Chromatogr Date: 1965-07

8. Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.

Authors: W A Schroeder; T H Huisman; J R Shelton; J B Shelton; E F Kleihauer; A M Dozy; B Robberson
Journal: Proc Natl Acad Sci U S A Date: 1968-06 Impact factor: 11.205

9. The "D" (13-15) trisomy syndrome: an analysis of 7 examples.

Authors: G J Snodgrass; L J Butler; N E France; L Crome; A Russell
Journal: Arch Dis Child Date: 1966-06 Impact factor: 3.791

10. Hemoglobin variations in D-trisomy syndrome.

Authors: M G Wilson; W A Schroeder; D A Graves; V D Kach
Journal: N Engl J Med Date: 1967-11-02 Impact factor: 91.245

18 in total

1. Nonrandom distribution of exchange points in patients with structural rearrangements.

Authors: Y Nakagome; H Chiyo
Journal: Am J Hum Genet Date: 1976-01 Impact factor: 11.025

2. BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

Authors: S A Latt; H F Willard; P S Gerald
Journal: Chromosoma Date: 1976-08-17 Impact factor: 4.316

10. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.

Authors: M Zatz; A M Vianna-Morgante; P Campos; A J Diament
Journal: J Med Genet Date: 1981-12 Impact factor: 6.318

Trisomy 13 with a 13-X translocation.

1. Studies on the induction of translocations in mouse spermatogonia. IV. Effects of acute gamma-irradiation.

2. Multiple abnormalities due to possible genetic inactivation in an X-autosome translocation.

3. Studies on the heterogeneity of hemoglobin. 13. Chromatography of various human and animal hemoglobin types on DEAE-Sephadex.

4. Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.

5. An improved method for quantitative determination of human fetal hemoglobin.

6. Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents.

7. Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins.

8. Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.

9. The "D" (13-15) trisomy syndrome: an analysis of 7 examples.

10. Hemoglobin variations in D-trisomy syndrome.

1. Nonrandom distribution of exchange points in patients with structural rearrangements.

2. BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes.

3. Investigation of the "variable spreading" of X inactivation into a translocated autosome.

4. Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.

5. Abnormal X chromosomes in man: origin, behavior and effects.

6. Partial trisomy 13q21toqter de novo due to a recombinant chromosome rec(13)dup q.

7. The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

8. The aetiology of the cat eye syndrome reconsidered.

9. X-autosome translocations: cytogenetic characteristics and their consequences.

10. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.