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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

6. A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.

Authors: F Nuzzo; A Marini; C Baglioni; C E Ford; L De Carli; L Piceni Sereni
Journal: Cytogenetics Date: 1968

7. A complex familial translocation involving chromosomes 5, 9 and 13.

Authors: K Fredga; B Hall
Journal: Cytogenetics Date: 1970

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. Familial transmission of a translocation between two non-homologous large acrocentric chromosomes. Clinical, cytogenetic and autoradiographic studies.

Authors: P Jacobsen; M Mikkelsen; A Froland; A Dupont
Journal: Ann Hum Genet Date: 1966-05 Impact factor: 1.670

10. Siblings with different types of chromosal aberrations due to D-E-translocation of the mother.

Authors: E Hauschteck; G Mürset; A Prader; E Bühler
Journal: Cytogenetics Date: 1966

15 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. Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.

Authors: C G Palmer; C Poland; T Reed; J Kojetin
Journal: Hum Genet Date: 1976-02-29 Impact factor: 4.132

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

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

4. Partial and complete trisomy 9: delineation of a trisomy 9 syndrome.

Authors: G R Sutherland; R F Carter; L L Morris
Journal: Hum Genet Date: 1976-05-19 Impact factor: 4.132

5. 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

6. 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 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

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

1. Identification of human chromosomes by DNA-binding fluorescent agents.

2. [Autoradiographic studies on DNA-replication of human mitotic chromosomes].

3. A case of trisomy 9.

4. [Cp trisomy: a new syndrome].

5. [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].