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Items: 3

1.

Girl with accelerated growth, hearing loss, inner ear anomalies, delayed myelination of the brain, and del(22)(q13.1q13.2).

Fujita Y, Mochizuki D, Mori Y, Nakamoto N, Kobayashi M, Omi K, Kodama H, Yanagawa Y, Abe T, Tsuzuku T, Yamanouchi Y, Takano T.

Am J Med Genet. 2000 May 29;92(3):195-9.

PMID:
10817654
2.

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.

Prasad C, Prasad AN, Chodirker BN, Lee C, Dawson AK, Jocelyn LJ, Chudley AE.

Clin Genet. 2000 Feb;57(2):103-9.

PMID:
10735630
3.

Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).

Romain DR, Goldsmith J, Cairney H, Columbano-Green LM, Smythe RH, Parfitt RG.

J Med Genet. 1990 Sep;27(9):588-9.

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