Literature DB >> 955626

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

H Fujita, M Shimazaki, T Takeuchi, Y Hayakawa, T Oura.   

Abstract

Marker chromosomes carried by unrelated 3 cases were identified as a part of No. 9 chromosome through the analysis of the chromatid fine structure after trypsin-giemsa treatment. They showed characteristic features of that 9p trisomic syndrome which were described by Rethoré et al. (1973). In addition to those features, some clinical and laboratory findings on growth hormon deficiency were disclosed in this report.

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Year:  1976        PMID： 955626     DOI： 10.1007/BF00270857

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


  12 in total

1.  Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).

Authors:  C Stoll; J M Levy; A Gardea
Journal:  Humangenetik       Date:  1975

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

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

3.  Banding in human chromosomes treated with trypsin.

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

4.  Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

Authors:  P E Podruch; B Weisskopf
Journal:  J Pediatr       Date:  1974-07       Impact factor: 4.406

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.  [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

7.  [Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].

Authors:  J Lejeuen; R Berger; M O Réthoré; C Salmon; M Kaplan
Journal:  Ann Genet       Date:  1966

8.  [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

9.  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

10.  Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.

Authors:  H Fujita; T Abe; K Yamamoto; J Furuyama
Journal:  Humangenetik       Date:  1974
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  4 in total

1.  Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).

Authors:  M Habedank; J Faust
Journal:  Hum Genet       Date:  1978-06-27       Impact factor: 4.132

2.  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

3.  Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis.

Authors:  Stefano Stagi; Elisabetta Lapi; Salvatore Seminara; Silvia Guarducci; Marilena Pantaleo; Sabrina Giglio; Francesco Chiarelli; Maurizio de Martino
Journal:  BMC Endocr Disord       Date:  2014-01-08       Impact factor: 2.763

4.  Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Authors:  Saadia Amasdl; Abdelhafid Natiq; Siham Chafai Elalaoui; Aziza Sbiti; Thomas Liehr; Abdelaziz Sefiani
Journal:  J Med Case Rep       Date:  2016-05-13
  4 in total

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