Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes

Author:

Hol Frans A.,Schepens Marga T.,van Beersum Sylvia E.C.,Redolfi Elena,Affer Maurizio,Vezzoni Paolo,Hamel Ben C.J.,Karnes Pamela S.,Mariman Edwin C.M.,Zucchi Ileana

Publisher

Elsevier BV

Subject

Genetics

Reference36 articles.

1. Yeast artificial chromosomes containing human Xq24–Xq28 DNA: Library construction and representation of probe sequences;Abidi;Genomics,1990

2. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am. J. Hum. Genet.,1992

3. Neural tube defects as an X-linked condition;Baraitser;Am. J. Med. Genet.,1984

4. A metric map of humans: 23,500 loci in 850 bands;Collins;Proc. Natl. Acad. Sci. USA,1996

5. Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency;Conley;J. Pediatr.,1991

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