Literature DB >> 4639227

An 18p21q translocation in a patient with presumptive "monosomy G".

M M Cohen, T I Putnam.   

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Year:  1972        PMID: 4639227     DOI: 10.1001/archpedi.1972.02110180110016

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


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  11 in total

1.  Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  A male infant with monosomy 21.

Authors:  Y Kaneko; T Ikeuchi; M Sasaki; Y Stakae; S Kuwajima
Journal:  Humangenetik       Date:  1975-08-29

3.  A 46,XY, del(18)(pter leads to p1 100:) cebocephalic child from a 46,XX,t(12;18)(18pter leads to 18 p 1100:: 12qter leads to 12pter) normal parent.

Authors:  G Johnson; R Bachman
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

Review 4.  Heart disease associated with deletion of the short arm of chromosome 18.

Authors:  W Pearl
Journal:  Pediatr Cardiol       Date:  1989       Impact factor: 1.655

5.  Monosomy 21: a new case confirmed by in situ hybridization.

Authors:  M C Pellissier; N Philip; M A Voelckel-Baeteman; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

6.  21 monosomy in a retarded female infant.

Authors:  K H Halloran; W R Breg; M J Mahoney
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

7.  An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.

Authors:  D S Borgaonkar; V A McKusick; P A Farber
Journal:  J Med Genet       Date:  1973-12       Impact factor: 6.318

8.  Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

Authors:  M C Phelan; C C Morton; R E Stevenson; R E Tanzi; G D Stewart; P C Watkins; J F Gusella; J A Amos
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

9.  Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.

Authors:  Z Chettouh; M F Croquette; B Delobel; S Gilgenkrants; C Leonard; C Maunoury; M Prieur; M O Rethoré; P M Sinet; M Chery
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

10.  18p--syndrome resulting from 14q/18q 'dicentric' fusion translocation.

Authors:  S J Funderburk; R S Sparkes; I Klisak
Journal:  Hum Genet       Date:  1977-11-10       Impact factor: 4.132

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