Literature DB >> 1561110

Dinucleotide repeat polymorphism at the D22S264 locus.

C Marineau1, M Aubry, J P Julien, G A Rouleau.   

Abstract

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Year:  1992        PMID： 1561110      PMCID： PMC312206     

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  10 in total

1.  Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.

Authors:  T H Shaikh; M L Budarf; L Celle; E H Zackai; B S Emanuel
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-06-11       Impact factor: 16.971

3.  Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defect.

Authors:  M Chessa; G Butera; P Bonhoeffer; L Iserin; J Kachaner; S Lyonnet; A Munnich; D Sidi; D Bonnet
Journal:  Heart       Date:  1998-02       Impact factor: 5.994

4.  Molecular genetics alterations and tumor behavior of sporadic vestibular schwannoma from the People's Republic of China.

Authors:  Liu-Guan Bian; Wuttipong Tirakotai; Qing-Fang Sun; Wei-Guo Zhao; Jian-Kang Shen; Qi-Zhong Luo
Journal:  J Neurooncol       Date:  2005-07       Impact factor: 4.130

5.  Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome.

Authors:  L H Seaver; J W Pierpont; R P Erickson; R L Donnerstein; S B Cassidy
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

6.  Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas.

Authors:  J Sainz; K Figueroa; M E Baser; S M Pulst
Journal:  Hum Genet       Date:  1996-01       Impact factor: 4.132

Review 7.  Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.

Authors:  S Demczuk; A Lévy; M Aubry; M F Croquette; N Philip; M Prieur; U Sauer; P Bouvagnet; G A Rouleau; G Thomas
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

8.  Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion.

Authors:  S Debrus; G Berger; A de Meeus; U Sauer; S Guillaumont; M Voisin; A Bozio; S Demczuk; A Aurias; P Bouvagnet
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

9.  Simple, rapid and inexpensive quantitative fluorescent PCR method for detection of microdeletion and microduplication syndromes.

Authors:  Martin Stofanko; Higgor Gonçalves-Dornelas; Pricila Silva Cunha; Heloísa B Pena; Angela M Vianna-Morgante; Sérgio Danilo Junho Pena
Journal:  PLoS One       Date:  2013-04-19       Impact factor: 3.240

10.  An obesogenic feedforward loop involving PPARγ, acyl-CoA binding protein and GABAA receptor.

Authors:  Gerasimos Anagnostopoulos; Omar Motiño; Sijing Li; Vincent Carbonnier; Hui Chen; Valentina Sica; Sylvère Durand; Mélanie Bourgin; Fanny Aprahamian; Nitharsshini Nirmalathasan; Romain Donne; Chantal Desdouets; Marcelo Simon Sola; Konstantina Kotta; Léa Montégut; Flavia Lambertucci; Didier Surdez; Grossetête Sandrine; Olivier Delattre; Maria Chiara Maiuri; José Manuel Bravo-San Pedro; Isabelle Martins; Guido Kroemer
Journal:  Cell Death Dis       Date:  2022-04-18       Impact factor: 9.685
  10 in total

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