Literature DB >> 1150257

A case of trisomy 9p in a family with translocation 9/15.

P Balícek, J Zizka, J Lichý.   

Abstract

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Year:  1975        PMID: 1150257     DOI: 10.1007/bf00278432

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


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  6 in total

1.  A simple method for R banding of human chromosomes, showing a pH-dependent connection between R and G bands.

Authors:  J Sehested
Journal:  Humangenetik       Date:  1974-01-22

2.  [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].

Authors:  M O Rethoré; H Hoehn; H D Rott; J Couturier; B Dutrillaux; J Lejeune
Journal:  Humangenetik       Date:  1973-04-16

3.  A simple technique for demonstrating centromeric heterochromatin.

Authors:  A T Sumner
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

4.  New technique for distinguishing between human chromosomes.

Authors:  A T Sumner; H J Evans; R A Buckland
Journal:  Nat New Biol       Date:  1971-07-07

5.  A new case of trisomy for the short arm of No. 9 chromosome.

Authors:  C Baccichetti; R Tenconi
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

6.  [On two familial cases of complex translocations].

Authors:  J Lejeune; R Burger
Journal:  Ann Genet       Date:  1965
  6 in total
  11 in total

1.  Possible intrachromosomal duplication in a case of trisomy 9p.

Authors:  H Chiyo; J Furuyama; N Suehara; Y Obashi; H Kikkawa
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

2.  Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975-12-23

3.  Trisomy 9p resulting from maternal 9/21 translocation.

Authors:  I Sŭbrt; B Blehová; B Pallová
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

4.  47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

Authors:  H Fujita; M Shimazaki; T Takeuchi; Y Hayakawa; T Oura
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

5.  De novo trisomy 9pter leads to q13.

Authors:  N B Kardon; H R Salwen; M A Krauss; J G Davis; E C Jenkins
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

Review 6.  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

7.  Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

Authors:  M Tolksdorf; J Kunze; G Gross-Selbeck; K Sperling; R D Wegner; V Wieczorek; M Vogel
Journal:  Eur J Pediatr       Date:  1977-08-23       Impact factor: 3.183

Review 8.  Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors:  P Jalbert; B Sele
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

9.  Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Authors:  P Jalbert; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

Review 10.  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

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