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12 in total

1. MEIOTIC AND MITOTIC STUDIES OF A FAMILIAL RECIPROCAL TRANSLOCATION BETWEEN TWO AUTOSOMES OF GROUP 6-12.

Authors: J LINDSTEN; M FRACCARO; H P KLINGER; P ZETTERQVIST
Journal: Cytogenetics Date: 1965

2. [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

3. [2 familial translocations occurring together in each of 2 sisters, one balanced, the other partial trisomic 10q].

Authors: J de Grouchy; C Finaz; M Roubin; J Roy
Journal: Ann Genet Date: 1972-06

4. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].

Authors: C Laurent; J M Robert; J Grambert; B Dutrillaux
Journal: Lyon Med Date: 1971-12-26

5. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].

Authors: J Lejeune; M O Rethoré; R Berger; D Abonyi; B Dutrillaux; G See
Journal: Ann Genet Date: 1968-09

6. [6-12 13-15 translocation and partial 6-12 trisomy (probably 10)].

Authors: J de Grouchy; J Canet
Journal: Ann Genet Date: 1965

7. New translocation in three generations of a family.

Authors: P Cooke
Journal: J Med Genet Date: 1968-09 Impact factor: 6.318

8. A translocation t (Bq+: Cq-) in a West Indian family and a report of a second family showing a possible long arm group B translocation.

Authors: M J Thornburn; E H Smith-Read; J E Peck
Journal: Arch Dis Child Date: 1969-02 Impact factor: 3.791

9. [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].

Authors: J De Grouchy; S Thieffry; J Aicardi; J J Chevrie; G Zucker
Journal: Arch Fr Pediatr Date: 1967-10

10. Familial reciprocal C/18 translocation.

Authors: H H Punnet; L Pinsky; A M Digeorge; R J Gorlin
Journal: Am J Hum Genet Date: 1966-11 Impact factor: 11.025

11 in total

1. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors: J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal: J Med Genet Date: 1986-10 Impact factor: 6.318

2. A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.

Authors: S W Soukup; W Yarema; M Robinow
Journal: Humangenetik Date: 1974

3. Brother and sister with trisomy 10p: a new syndrome.

Authors: E Schleiermacher; U Schliebitz; C Steffens
Journal: Humangenetik Date: 1974

4. Terminal deletion of (1)(q42) and its phenotypical manifestations.

Authors: M Andrle; A Erlach; W R Mayr; A Rett
Journal: Hum Genet Date: 1978-02-23 Impact factor: 4.132

5. Partial trisomy 10q: a recognizable syndrome.

Authors: J M Klep-de Pater; J B Bijlsma; H F de France; N J Leschot; M Duijndam-van den Berge; J O van Hemel
Journal: Hum Genet Date: 1979-01-19 Impact factor: 4.132

6. Trisomy 12p due to familial t(12p-,6q plus) translocation.

Authors: J P Fryns; H Van Den Berghe
Journal: Humangenetik Date: 1974

7. Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Characterization of the region responsible for the partial trisomy 10q syndrome.

Authors: R Miró; C Templado; M Ponsá; J Serradell; S Marina; J Egozcue
Journal: Hum Genet Date: 1980-02 Impact factor: 4.132

[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].