Literature DB >> 4547938

[Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].

B Dallapiccola, L Capra, G Preto, M Covic, B Dutrillaux.   

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Year:  1974        PMID: 4547938

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


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  13 in total

1.  Hand dermatoglyphics in trisomy 4p.

Authors:  P Mastroiacovo; V Currò; A Calabro; B Dallapiccola
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

2.  A case of trisomy of the short arms of chromosome no. 4 with translocation t(4p 21p; 4q 21q) in the mother.

Authors:  M Furbetta; G Rosi; P Cossu; A Cao
Journal:  Humangenetik       Date:  1975

3.  Nonrandom distribution of exchange points in patients with structural rearrangements.

Authors:  Y Nakagome; H Chiyo
Journal:  Am J Hum Genet       Date:  1976-01       Impact factor: 11.025

4.  [Trisomy 4p. Three new observations (author's transl)].

Authors:  F Giraud; J F Mattei; M G Mattei; S Ayme; R Bernard
Journal:  Humangenetik       Date:  1975-11-06

5.  The radiological pattern associated with the trisomy of the short arm of chromosome No 4.

Authors:  B Dallapiccola; G Giovannelli; A Forabosco
Journal:  Pediatr Radiol       Date:  1975-01-24

6.  A homozygote for pericentric inversion of chromosome 4.

Authors:  N J Carpenter; B Say; N D Barber
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

7.  A fetus with recombinant of chromosome 8 inherited from her carrier father.

Authors:  A Fujimoto; J W Towner; S B Turkel; M G Wilson
Journal:  Hum Genet       Date:  1978-02-16       Impact factor: 4.132

Review 8.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.

Authors:  H Schröchsnadel; C Feichtinger; C Scheminzky
Journal:  Humangenetik       Date:  1975-10-07

10.  Duplication deficiency as the result of meiotic segregation of a maternal InV (10).

Authors:  E Yunis; O Torres de Caballero
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

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