Pages that link to "Q72022882"
Jump to navigation
Jump to search
The following pages link to Steroid sulfatase activity in cultured fibroblasts of XX males (Q72022882):
Displaying 15 items.
- Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids (Q35199786) (← links)
- Steroid sulfatase gene in XX males (Q35201343) (← links)
- Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency). (Q36127399) (← links)
- On the genetic length of the short arm of the human X chromosome (Q40138739) (← links)
- Genetic aspects of H-Y antigen (Q40316413) (← links)
- Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism (Q48828636) (← links)
- Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome (Q58194253) (← links)
- Evidence for X-linkage and non-inactivation of steroid sulphatase locus in wood lemming (Q59087017) (← links)
- Steroid sulphatase levels in XX males, including observations on two affected cousins (Q60641520) (← links)
- Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome (Q67285690) (← links)
- Pairing of X and Y chromosomes, non-inactivation of X-linked genes, and the maleness factor (Q70427828) (← links)
- Cytologic evidence for three human X-chromosomal segments escaping inactivation (Q71229923) (← links)
- Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation (Q71639110) (← links)
- Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype (Q71846112) (← links)
- Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations (Q72021198) (← links)