| Q69369480 | A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome |
| Q51791869 | Clinical features of incontinentia pigmenti with emphasis on oral and dental abnormalities. |
| Q33596991 | De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies |
| Q42557192 | De novo mutation in three families with multigenerational incontinentia pigmenti |
| Q34003452 | Dermatologic clues to inherited disease |
| Q37636776 | Dermatology and the human gene map. |
| Q41090403 | Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation |
| Q61040936 | Expression of eotaxin, an eosinophil-selective chemokine, parallels eosinophil accumulation in the vesiculobullous stage of incontinentia pigmenti |
| Q42500319 | Familial linear and whorled nevoid hypermelanosis |
| Q40866170 | Female mice heterozygous for IKK gamma/NEMO deficiencies develop a dermatopathy similar to the human X-linked disorder incontinentia pigmenti |
| Q50251708 | Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko |
| Q28266551 | Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28 |
| Q33682795 | Gonadal mosaicism for incontinentia pigmenti in a healthy male |
| Q33683279 | Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis |
| Q55483105 | Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17). |
| Q33922438 | Hypomelanosis of ito and a 'mirror image' whole chromosome duplication resulting in trisomy 14 mosaicism |
| Q33594861 | Incontinentia pigmenti (Bloch-Sulzberger syndrome). |
| Q44967044 | Incontinentia pigmenti associated with bilateral cleft lip and palate |
| Q36677582 | Incontinentia pigmenti in boys: a series and review of the literature |
| Q53773660 | Incontinentia pigmenti: late sequelae and genotypic diagnosis: a three-generation study of four patients. |
| Q33596604 | Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2. |
| Q30502692 | Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase |
| Q67913542 | Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers |
| Q35195848 | Localization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints |
| Q30495385 | Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders |
| Q88132766 | Multimodal Retinal Imaging in Incontinentia Pigmenti Including Optical Coherence Tomography Angiography: Findings From an Older Cohort With Mild Phenotype |
| Q51651779 | Retinal and other manifestations of incontinentia pigmenti (Bloch-Sulzberger syndrome). |
| Q33596839 | Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasia |
| Q35644329 | The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region. |
| Q34530723 | The results of early physiotherapy on a child with incontinentia pigmenti with encephalocele |
| Q72214747 | Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11 |
| Q59161660 | Unusual Neonatal Presentation of Incontinentia Pigmenti with Persistent Pulmonary Hypertension of the Newborn: A Case Report |
| Q33683330 | X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of Xp. |
| Q33594410 | X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease |
| Q67941705 | X linked mental retardation |
| Q74582606 | X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation |
| Q51983447 | X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28. |
| Q64045307 | [Incontinentia pigmenti: a case study] |