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Items: 4

1.

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A.

Hum Genet. 2001 Sep;109(3):286-94.

PMID:
11702209
2.
3.

Xp deletions associated with autism in three females.

Thomas NS, Sharp AJ, Browne CE, Skuse D, Hardie C, Dennis NR.

Hum Genet. 1999 Jan;104(1):43-8.

PMID:
10071191
4.

Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.

Magenis RE, Webb MJ, McKean RS, Tomar D, Allen LJ, Kammer H, Van Dyke DL, Lovrien E.

Hum Genet. 1982;62(3):271-6.

PMID:
6892019
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