The question of trisomy 22 syndrome

Author:

Goodman R.M.,Katznelson M. Bat-Miriam,Spero M.,Shaki R.,Padeh B.,Sadan N.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference8 articles.

1. Le probleme de la trisomie 22;Walbaum;Pediatrica,1970

2. Familial occurrence of trisomy 22;Uchida;Amer. J. Hum. Genet.,1968

3. A probable case of incomplete trisomy of a chromosome of the 13–15 group;Ishmael;J. Med. Genet.,1965

4. Trisomy G without Down's syndrome;Sparkes;Lancet,1966

5. Another child with 47 chromosomes;Ferguson;Med. J. Aust.,1963

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1. DERMATOGLYPHICS IN THE G DELETION SYNDROMES*;Journal of Intellectual Disability Research;2008-06-28

2. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome;Clinical Genetics;2008-04-23

3. Complete trisomy 22;Clinical Genetics;2008-04-23

4. Trisomy 22 with holoprosencephaly: A clinicopathologic study;Teratology;1990-10

5. A case of partial trisomy 22 resulting from maternal 11/22 translocation;Japanese journal of human genetics;1979-12

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