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Results: 3

PubMed Links for Books (Select 2981074)

1.

Twelve new patients with 13q deletion syndrome: genotype-phenotype analyses in progress.

Quélin C, Bendavid C, Dubourg C, de la Rochebrochard C, Lucas J, Henry C, Jaillard S, Loget P, Loeuillet L, Lacombe D, Rival JM, David V, Odent S, Pasquier L.

Eur J Med Genet. 2009 Jan-Feb;52(1):41-6. doi: 10.1016/j.ejmg.2008.10.002. Epub 2008 Oct 31.

PMID:
19022413
2.

13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.

Ballarati L, Rossi E, Bonati MT, Gimelli S, Maraschio P, Finelli P, Giglio S, Lapi E, Bedeschi MF, Guerneri S, Arrigo G, Patricelli MG, Mattina T, Guzzardi O, Pecile V, Police A, Scarano G, Larizza L, Zuffardi O, Giardino D.

J Med Genet. 2007 Jan;44(1):e60.

3.

Tandem triplication of chromosome 13q14 with inverted interstitial segment in a 4 year old girl.

Brecevic L, Basaran S, Dutly F, Röthlisberger B, Schinzel A.

J Med Genet. 2000 Dec;37(12):964-7. No abstract available.

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