Regional mapping of the parathyroid hormone gene (...[Cytogenet Cell Genet. 1991]

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1: Cytogenet Cell Genet. 1991;56(2):103-4.Links

Regional mapping of the parathyroid hormone gene (PTH) by cytogenetic and molecular studies.

Tonoki H, Narahara K, Matsumoto T, Niikawa N.

Department of Pediatrics, Hokkaido University School of Medicine, Sapporo, Japan.

The locus for the human parathyroid hormone gene (PTH) was assigned to a region proximal to 11p15.4 using restriction fragment length polymorphisms and gene dose studies performed on a patient with the Beckwith-Wiedemann syndrome accompanied with a chromosome abnormality [46,XX,-14,+der(14),t(14;11)(q32.3;p15.3)pat]. Our data suggest that PTH is localized in 11p15.3----p15.1, most likely near the border of the bands 11p15.4 and 11p15.3.

PMID: 1672845 [PubMed - indexed for MEDLINE]

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.
Genomics. 1990 Dec; 8(4):693-8.

[Genomics. 1990]
Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11.
Eur J Pediatr. 1992 Jul; 151(7):511-4.

[Eur J Pediatr. 1992]
Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
Am J Med Genet. 1994 Feb 15; 49(4):378-83.

[Am J Med Genet. 1994]
ReviewPaternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.
J Med Genet. 1997 Oct; 34(10):819-26.

[J Med Genet. 1997]
ReviewPaternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature.
Cancer Genet Cytogenet. 1992 Jan; 58(1):66-70.

[Cancer Genet Cytogenet. 1992]
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Cited by 3 PubMed Central articles

ReviewPaternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.
Slavotinek A, Gaunt L, Donnai D. J Med Genet. 1997 Oct; 34(10):819-26.

[J Med Genet. 1997]
Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).
Tommerup N, Brandt CA, Pedersen S, Bolund L, Kamper J. J Med Genet. 1993 Nov; 30(11):958-61.

[J Med Genet. 1993]
Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females.
Moutou C, Junien C, Henry I, Bonaïti-Pellié C. J Med Genet. 1992 Apr; 29(4):217-20.

[J Med Genet. 1992]

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