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8 in total

1. Clinical and behavioural profile of a rare variant of Klinefelter syndrome-48, XXXY.

Authors: A Venkateshwari; A Srilekha; Ashrafunnisa Begum; M Sujatha; P Usha Rani; T Sunitha; Pratibha Nallari; A Jyothy
Journal: Indian J Pediatr Date: 2010-01-20 Impact factor: 1.967

2. Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy.

Authors: T Hassold; D Pettay; K May; A Robinson
Journal: Hum Genet Date: 1990-10 Impact factor: 4.132

3. Origin of 48,XXXY: the evidence of the Xg blood groups.

Authors: R A Pfeiffer; R Sanger
Journal: J Med Genet Date: 1973-06 Impact factor: 6.318

4. Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY.

Authors: J L Simpson; G Morillo-Cucci; M Horwith; F H Stiefel; F Feldman; J German
Journal: Humangenetik Date: 1974-03-28

5. [XXXY Klinefelter's syndrome].

Authors: W Vormittag; M Weninger
Journal: Humangenetik Date: 1972

6. The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.

Authors: P Barlow
Journal: Humangenetik Date: 1973

7. XXXX syndrome: case report, and a note on genetic counselling and fertility.

Authors: R J Gardner; A M Veale; V E Sands; M D Holdaway
Journal: Humangenetik Date: 1973

8. Parental origin of the extra chromosomes in polysomy X.

Authors: C A Leal; J W Belmont; R Nachtman; J M Cantu; C Medina
Journal: Hum Genet Date: 1994-10 Impact factor: 4.132

8 in total