| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00271160 |
| P698 | PubMed publication ID | 7196380 |
| P2093 | author name string | F D Bricarelli | |
| U Müller | |||
| J Lindsten | |||
| U Wolf | |||
| L D Carbone | |||
| M Fraccaro | |||
| H Ringertz | |||
| A Hjerpe | |||
| A Mayerová | |||
| E M Ritzén | |||
| F Lindgren | |||
| P Baggio | |||
| C Sicchero | |||
| D C Rovetta | |||
| P2860 | cites work | XY gonadal dysgenesis and the H-Y antigen. Report on 12 cases | Q39671099 |
| Familial XX true hermaphroditism and the H-Y antigen | Q39671110 | ||
| International nomenclature of constitutional diseases of bone with bibliography | Q39823711 | ||
| The mechanism of gonadal differentiation | Q40196507 | ||
| Binding studies of H-Y antigen in rat tissues: indications for a gonad-specific receptor | Q40688219 | ||
| A highly sensitive peroxidase-antiperoxidase method for detection of H-Y antigen on cultivated human fibroblasts | Q41157309 | ||
| Campomelic dysplasia. Further elucidation of a distinct entity. | Q52299172 | ||
| Increasing frequency of a syndrome of multiple osseous defects? | Q52331767 | ||
| Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal | Q67013316 | ||
| Recessive sex-determining genes in human XX male syndrome | Q67017333 | ||
| Recessive male-determining genes | Q67390811 | ||
| Familial camptomelic dwarfism | Q69590885 | ||
| A gene controlling H-Y antigen on the X chromosome. Tentative assignment by deletion mapping to Xp223 | Q71240329 | ||
| Turner syndrome patients are H-Y positive | Q71267631 | ||
| [The campomelic syndrome] | Q71786081 | ||
| P433 | issue | 1 | |
| P921 | main subject | campomelic dysplasia | Q1031536 |
| P304 | page(s) | 15-22 | |
| P577 | publication date | 1981-01-01 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Sex-reversed XY females with campomelic dysplasia are H-Y negative | |
| P478 | volume | 57 |
| Q24517890 | A clinical and genetic study of campomelic dysplasia |
| Q69410608 | Acampomelic campomelic dysplasia |
| Q28261277 | Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1 |
| Q70680724 | Campomelic dysplasia--an underdiagnosed condition? |
| Q24656897 | Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia |
| Q70587583 | Determination of the H-Y antigen in amniotic cells. Its use in prenatal diagnosis |
| Q70475322 | Diagnostic application of first trimester trophoblast sampling in 100 pregnancies |
| Q52277764 | Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings. |
| Q40316413 | Genetic aspects of H-Y antigen |
| Q71086933 | H-Y antigen studies in thirty patients with abnormal gonadal differentiation: Correlations among sex chromosome complement, H-Y antigen, and gonadal type |
| Q51772817 | Novel SOX9 gene mutation in campomelic dysplasia with autosomal sex reversal. |
| Q70338538 | Ovarian development in 46,XY gonadal dysgenesis |
| Q39804165 | Radiology and histopathology of the bent limbs in campomelic dysplasia: implications in the aetiology of the disease and review of theories |
| Q40175004 | Variability in serologically detected male antigen titer and some resulting problems: A critical review |
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