Literature DB >> 6873114

21-Monosomy in a liveborn male infant.

R Herva, M Koivisto, U Seppänen.   

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Year:  1983        PMID： 6873114     DOI： 10.1007/bf00661907

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  9 in total

1.  A male infant with monosomy 21.

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

2.  [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

Authors:  J LEJEUNE; R BERGER; M O RETHORE; L ARCHAMBAULT; H JEROME; S THIEFFRY; J AICARDI; M BROYER; J LAFOURCADE; J CRUVEILLER; R TURPIN
Journal:  C R Hebd Seances Acad Sci       Date:  1964-11-30

3.  A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-.

Authors:  J G Davis; E C Jenkins; H P Klinger; R G Weed
Journal:  Cytogenet Cell Genet       Date:  1976

4.  Full monosomy 21: a clinically recognizable syndrome?

Authors:  J P Fryns; F D'Hondt; P Goddeeris; H van den Berghe
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

5.  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

6.  Monosomy 21 in spontaneous abortus.

Authors:  K Ohama; T Kajii
Journal:  Humangenetik       Date:  1972

7.  A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.

Authors:  U Gripenberg; J Elfving; L Gripenberg
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

8.  Anatomic and chromosomal anomalies in 639 spontaneous abortuses.

Authors:  T Kajii; A Ferrier; N Niikawa; H Takahara; K Ohama; S Avirachan
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

9.  Unbalanced 13q/21q translocation: a revised study of the case previously reported as 21-monosomy.

Authors:  T Ikeuchi; I Kondo; M Sasaki; Y Kaneko; S Kodama
Journal:  Hum Genet       Date:  1976-08-30       Impact factor: 4.132
  9 in total
  3 in total

1.  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

2.  Monosomy 21 seen in live born is unlikely to represent true monosomy 21: a case report and review of the literature.

Authors:  Trent Burgess; Lilian Downie; Mark D Pertile; David Francis; Melissa Glass; Sara Nouri; Rosalynn Pszczola
Journal:  Case Rep Genet       Date:  2014-02-04

3.  Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development.

Authors:  Cathrine Jespersgaard; Ida N Damgaard; Nanna Cornelius; Iben Bache; Niels Knabe; Maria J Miranda; Zeynep Tümer
Journal:  Mol Cytogenet       Date:  2016-02-04       Impact factor: 2.009
  3 in total

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