Literature DB >> 4691464

A "G" deletion syndrome anti-mongolism.

H G Richmond, P MacArthur, D Hunter.   

Abstract

Mesh：

Year:  1973        PMID： 4691464     DOI： 10.1111/j.1651-2227.1973.tb08096.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  10 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.  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

3.  Clinical and cytogenetic studies of two infants with partial monosomy G.

Authors:  T Maeda; M Ohno; H Nishida
Journal:  Hum Genet       Date:  1977-03-14       Impact factor: 4.132

4.  Four new cases of ring 21 and 22 including familial transmission of ring 21.

Authors:  C G Palmer; M E Hodes; T Reed; J Kojetin
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

5.  "Compensatory" uniparental disomy of chromosome 21 in two cases.

Authors:  O Bartsch; M B Petersen; I Stuhlmann; G Mau; M Frantzen; E Schwinger; S E Antonarakis; M Mikkelsen
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

6.  Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit?

Authors:  J L García Miranda; A Otero Gómez; H Varela Ansedes; N Rancel Torres; C González Espinosa; C Cortabarría; G Sánchez Salgado
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

7.  Partial monosomy 13 and 21 due to a familial 13/21 translocation.

Authors:  P G Otto; S Toledo; A Richieri-Costa; P A Otto; A M Vianna-Morgante; S Kasahara
Journal:  Hum Genet       Date:  1978-04-24       Impact factor: 4.132

8.  Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.

Authors:  M Mikkelsen; S Vestermark
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

9.  46,XY/46,XY,21q- mosaicism in an infant with neutropenia and properdin deficiency.

Authors:  R L Neu; J A Stockman; R E Spitzer; R H Tomar
Journal:  J Med Genet       Date:  1976-08       Impact factor: 6.318

10.  Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature.

Authors:  Svetlana G Vorsanova; Ivan Y Iourov; Victoria Y Voinova-Ulas; Anja Weise; Victor V Monakhov; Alexei D Kolotii; Ilia V Soloviev; Petr V Novikov; Yuri B Yurov; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2008-06-19       Impact factor: 2.009
  10 in total

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