Literature DB >> 4774540

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

C Baccichetti, R Tenconi.   

Abstract

Mesh:

Year:  1973        PMID: 4774540      PMCID: PMC1013037          DOI: 10.1136/jmg.10.3.296

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


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  5 in total

1.  [A new technic of analysis of the human karyotype].

Authors:  B Dutrillaux; J Lejeune
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1971-05-17

2.  [Cp trisomy: a new syndrome].

Authors:  J M Canu; L Buentello; S Armendares
Journal:  Ann Genet       Date:  1971-09

3.  [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].

Authors:  M O Rethoré; L Larget-Piet; D Abonyi; M Boeswillwald; R Berger; S Carpentier; J Cruveiller; B Dutrillau; J Lafourcade; M Penneau; J Lejeune
Journal:  Ann Genet       Date:  1970-12

4.  [Partial trisonomy C9 in a case of balanced maternal B4-C9 translocation].

Authors:  H D Rott; G Schwanitz; K P Grosse
Journal:  Z Kinderheilkd       Date:  1971

5.  Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

Authors:  H Hoehn; W Engel; H Reinwein
Journal:  Humangenetik       Date:  1971
  5 in total
  12 in total

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

Authors:  P Balícek; J Zizka; J Lichý
Journal:  Humangenetik       Date:  1975

2.  A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).

Authors:  M K Mason; D A Spencer; A Rutter
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

3.  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

4.  A case of trisomy for the short arm of chromosome no. 9(+9(p)).

Authors:  M E Käosaar; A V Mikelsaar; T A Talvik; R V Mikelsaar
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

5.  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

6.  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

Review 7.  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

8.  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

9.  Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).

Authors:  V B Penehaszadeh; R Coco
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

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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