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6 in total

1. A deletion in chromosome 22 can cause DiGeorge syndrome.

Authors: A de la Chapelle; R Herva; M Koivisto; P Aula
Journal: Hum Genet Date: 1981 Impact factor: 4.132

2. Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen----q131) and adenosine deaminase (q131----qter) on chromosome 20.

Authors: T Mohandas; R S Sparkes; E J Suh; M S Hershfield
Journal: Hum Genet Date: 1984 Impact factor: 4.132

3. Assignment of the glyoxalase II gene (HAGH) to human chromosome 16.

Authors: N K Honey; T B Shows
Journal: Hum Genet Date: 1981 Impact factor: 4.132

4. Mapping studies of the serum cholinesterase-2 locus (CHE2).

Authors: M L Marazita; B J Keats; M A Spence; R S Sparkes; L L Field; M C Sparkes; M Crist
Journal: Hum Genet Date: 1989-09 Impact factor: 4.132

5. Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16.

Authors: H P Koeffler; R S Sparkes; H Stang; T Mohandas
Journal: Proc Natl Acad Sci U S A Date: 1981-11 Impact factor: 11.205

6. Regional gene assignment of human porphobilinogen deaminase and esterase A4 to chromosome 11q23 leads to 11qter.

Authors: A L Wang; F X Arredondo-Vega; P F Giampietro; M Smith; W F Anderson; R J Desnick
Journal: Proc Natl Acad Sci U S A Date: 1981-09 Impact factor: 11.205

6 in total