Correa-Cerro L, Rivera H, Vasquez A
J Med Genet. 1997; 34(2):161-3.
PMID: 9039996
PMC: 1050873.
DOI: 10.1136/jmg.34.2.161.
Hatchwell E, Robinson D, Crolla J, Cockwell A
J Med Genet. 1996; 33(3):216-20.
PMID: 8728694
PMC: 1051870.
DOI: 10.1136/jmg.33.3.216.
Hatchwell E
J Med Genet. 1996; 33(3):177-83.
PMID: 8728687
PMC: 1051863.
DOI: 10.1136/jmg.33.3.177.
Steichen-Gersdorf E, Trawoger R, Duba H, Mayr U, Felber S, Utermann G
Hum Genet. 1993; 90(6):611-3.
PMID: 8444466
DOI: 10.1007/BF00202477.
Landy S, Donnai D
J Med Genet. 1993; 30(1):53-9.
PMID: 8423608
PMC: 1016235.
DOI: 10.1136/jmg.30.1.53.
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.
Tommerup N
J Med Genet. 1993; 30(9):713-27.
PMID: 8411066
PMC: 1016528.
DOI: 10.1136/jmg.30.9.713.
Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.
Hyden-Granskog C, Salonen R, von Koskull H
Hum Genet. 1993; 91(2):185-9.
PMID: 8096494
DOI: 10.1007/BF00222723.
Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.
Wolff D, Brown C, Schwartz S, Duncan A, Surti U, Willard H
Am J Hum Genet. 1994; 55(1):87-95.
PMID: 8023855
PMC: 1918222.
Incontinentia pigmenti nomenclature.
Sybert V
Am J Hum Genet. 1994; 55(1):209-11.
PMID: 8023849
PMC: 1918241.
Generation of a human X-derived minichromosome using telomere-associated chromosome fragmentation.
Farr C, Bayne R, Kipling D, Mills W, Critcher R, Cooke H
EMBO J. 1995; 14(21):5444-54.
PMID: 7489733
PMC: 394653.
DOI: 10.1002/j.1460-2075.1995.tb00228.x.
Two cases of X/autosome translocation in females with incontinentia pigmenti.
Hodgson S, Neville B, Jones R, Fear C, Bobrow M
Hum Genet. 1985; 71(3):231-4.
PMID: 4065895
DOI: 10.1007/BF00284581.
Tentative assignment of hypomelanosis of Ito to 9q33----qter.
Happle R
Hum Genet. 1987; 75(1):98-9.
PMID: 3804339
DOI: 10.1007/BF00273854.
Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1.
Turleau C, Taillard F, Doussau de Bazignan M, Delepine N, Desbois J, de Grouchy J
Hum Genet. 1986; 74(2):185-7.
PMID: 3464561
DOI: 10.1007/BF00282090.
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.
Sefiani A, Sinnett D, Abel L, Heuertz S, Craig I, Fraser N
Hum Genet. 1988; 80(3):282-6.
PMID: 3192215
DOI: 10.1007/BF01790098.
Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.
Yang-Feng T, DeGennaro L, Francke U
Proc Natl Acad Sci U S A. 1986; 83(22):8679-83.
PMID: 3095840
PMC: 386994.
DOI: 10.1073/pnas.83.22.8679.
Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases.
Crolla J, Gilgenkrantz S, de Grouchy J, Kajii T, Bobrow M
Hum Genet. 1989; 81(3):269-72.
PMID: 2921037
DOI: 10.1007/BF00279002.
Selection against lethal alleles in females heterozygous for incontinentia pigmenti.
MIGEON B, Axelman J, de Beur S, Valle D, Mitchell G, Rosenbaum K
Am J Hum Genet. 1989; 44(1):100-6.
PMID: 2562819
PMC: 1715454.
Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.
Read A, Donnai D
Am J Hum Genet. 1990; 47(1):166-8.
PMID: 2349946
PMC: 1683754.
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.
Temple I, Hurst J, Hing S, Butler L, Baraitser M
J Med Genet. 1990; 27(1):56-8.
PMID: 2308156
PMC: 1016883.
DOI: 10.1136/jmg.27.1.56.
The critical region on the human Xq.
THERMAN E, Laxova R, Susman B
Hum Genet. 1990; 85(5):455-61.
PMID: 2227929
DOI: 10.1007/BF00194216.