| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0888-7543(05)80219-8 |
| P698 | PubMed publication ID | 1427846 |
| P50 | author | Susan Lindsay | Q67405761 |
| P2093 | author name string | S S Bhattacharya | |
| A Curtis | |||
| O Williams | |||
| M E Porteous | |||
| S Kamakari | |||
| D Goudie | |||
| P2860 | cites work | A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 |
| A familial syndrome of short stature associated with facial dysplasia and genital anomalies | Q28253439 | ||
| Aarskog syndrome | Q33596494 | ||
| Use of restriction enzymes to detect potential gene sequences in mammalian DNA. | Q35079757 | ||
| Autosomal dominant inheritance of the Aarskog syndrome | Q40150527 | ||
| Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255]. | Q40391880 | ||
| Simple sequences are ubiquitous repetitive components of eukaryotic genomes. | Q40455691 | ||
| Report of the committee on the genetic constitution of the X chromosome | Q57405682 | ||
| Aarskog syndrome: full male and female expression associated with an X-autosome translocation | Q71316271 | ||
| P433 | issue | 2 | |
| P921 | main subject | Aarskog syndrome | Q303123 |
| P304 | page(s) | 298-301 | |
| P577 | publication date | 1992-10-01 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13) | |
| P478 | volume | 14 |
| Q48070907 | Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene |
| Q72667525 | Definition and mapping of STSs at STR and RFLP loci in Xp11-Xq22 |
| Q24336343 | Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor |
| Q38839147 | Minireview: Role of genetic changes of faciogenital dysplasia protein 1 in human disease |
| Q35882720 | PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28 |
| Q37843989 | Podosomal proteins as causes of human syndromes: a role in craniofacial development? |
| Q72209605 | X chromosome linkage studies in familial Rett syndrome |
| Q73013123 | X-linked mental retardation |
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