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Figure 5 | Orphanet Journal of Rare Diseases

Figure 5

From: Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci

Figure 5

Diagram of 22q11.1-q11.23 chromosomal region. Schematic representation of the 22q11.1-q11.23 chromosomal region between 15 and 23 Mb from the telomeric end of the short arm. Dark gray box represents the ~3Mb most common 22q11 deletion associated with DGS syndrome; white boxes represent the maximum distance between undeleted markers in this current study (case 4) and the previously reported MRKH cases. Light gray box shows the smallest 22q11.2 deletion common to known MRKH syndrome patients.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172