Regular ArticleIdentification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes
References (37)
- et al.
Yeast artificial chromosomes containing human Xq24–Xq28 DNA: Library construction and representation of probe sequences
Genomics
(1990) - et al.
Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency
J. Pediatr.
(1991) - et al.
YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers
Genomics
(1996) - et al.
Human elongation factor EF-1β: Cloning and characterization of the EF1β 5a gene and assignment of EF-1β isoforms to chromosomes 2, 5, 15, and X
Biochem. Biophys. Res. Commun.
(1993) - et al.
Mapping of the MYCL2 processed gene to Xq22–23 and identification of an additional L MYC-related sequence in Xq27.2
FEBS Lett.
(1999) - et al.
Transcription map of Xq27: Candidates for several X-linked diseases
Genomics
(1999) - et al.
YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter
Genomics
(1996) - et al.
Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
Am. J. Hum. Genet.
(1992) - et al.
Neural tube defects as an X-linked condition
Am. J. Med. Genet.
(1984) - et al.
A metric map of humans: 23,500 loci in 850 bands
Proc. Natl. Acad. Sci. USA
(1996)
Sublocalization of the synovial sarcoma-associated t(X;18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization
Oncogene
(1993)
Lumbosacral spina bifida and myeloschizis in a female foetus with de novo X/autosomal translocation (t(X;22) (q27;q121))
Genet. Couns.
(1996)
Fibroblast growth factor homologous factor 2 (FHF2): Gene structure, expression and mapping to the Borjeson–Forssman–Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient
Hum. Genet.
(1999)
Cytogenetic and molecular studies of a duplication of Xq26 and Xq27 in two brothers with neural tube defects
Am. J. Hum. Genet.
(1993)
X-Linked Mental Retardation, a Clinical and Molecular Study
(1999)
Familial X-linked mental retardation and isolated growth hormone deficiency: Clinical and molecular findings
Am. J. Med. Genet.
(1996)
Genetic landmarks for defects in mouse neural tube closure
Teratology
(1997)
A family showing apparent X linked inheritance of both anencephaly and spina bifida
J. Med. Genet.
(1988)
Cited by (0)
- 1
To whom correspondence should be addressed. Telephone: +31.24.3614017. Fax: +31.24.3540488. E-mail: [email protected].
Copyright © 2000 Academic Press. All rights reserved.