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Literature DB >> 4140836

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

J P Fryns, H Van Den Berghe.

Abstract

Entities: Disease

Mesh：

Year: 1974 PMID： 4140836

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

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26 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. Partial trisomy of chromosome 11: a case report.

Authors: R E Falk; R E Carrel; M Valente; B F Crandall; R S Sparkes
Journal: Am J Ment Defic Date: 1973-01

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 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

5. New translocation in three generations of a family.

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

6. A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-).

Authors: G J Bargman; R L Neu; H O Powers; L I Gardner
Journal: J Med Genet Date: 1970-03 Impact factor: 6.318

7. 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

8. Two familial translocations involving the 6-12 group. With meiotic studies in one.

Authors: A McDermott; J Insley; D I Rushton; J H Edwards
Journal: Teratology Date: 1968-05

9. [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

10. [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 in total

1. Syndrome +12p. Case report and review.

Authors: R Tenconi; E Piovan; A Preto; R Magnabosco; C Baccichetti
Journal: Hum Genet Date: 1977-11-02 Impact factor: 4.132

2. Two cases of trisomy 12p due to rcpt (12;21)(p11;p11) inherited through three generations.

Authors: M Parslow; D Chambers; M Drummond; W Hunter
Journal: Hum Genet Date: 1979-04-05 Impact factor: 4.132

3. A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat.

Authors: H Nielsen; M Vetner; V Holm; S Askjaer; E Reske-Nielsen
Journal: Hum Genet Date: 1977-03-14 Impact factor: 4.132

4. Translocations involving chromosome 12. I. A report of a 12,21 translocation in a woman with recurrent abortions, and a study of the breakpoints and modes of ascertainment of translocations involving chromosome 12.

Authors: J H Ford; R H Rofe; R P Pavy
Journal: Hum Genet Date: 1981 Impact factor: 4.132