More precise localization of the human Factor IX gene by in situ hybridization

Quirk, Stephen; Chou, William; Polakowska, Renata; Zain, Sayeeda; Young, Frank E.; Doherty, Richard A.

doi:10.1159/000132119

Cited by 11 publications

(1 citation statement)

References 2 publications

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“…1984;Jagadeeswaran et al 1984). Buckle, Craig and Edwards (HGM8) and Quirk et al (1985) have also concluded from i_n situ experiments that F9 lies in the proximal part of the Xq27 band.…”

Section: New Gene and Pseudogene Assignmentsmentioning

confidence: 94%

Report of the committee on the genetic constitution of the X and Y chromosomes

Goodfellow¹,

Davies²,

Ropers³

1985

Cytogenet Genome Res

232

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“…1984;Jagadeeswaran et al 1984). Buckle, Craig and Edwards (HGM8) and Quirk et al (1985) have also concluded from i_n situ experiments that F9 lies in the proximal part of the Xq27 band.…”

Section: New Gene and Pseudogene Assignmentsmentioning

confidence: 94%

Report of the committee on the genetic constitution of the X and Y chromosomes

Goodfellow¹,

Davies²,

Ropers³

1985

Cytogenet Genome Res

232

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Bibliography on X‐linked mental retardation and related subjects III (1986)

et al. 1986

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J .M. 0. ) As promised i n a previous issue, from tims t o tim we s h a l l provide t h e readers of the American Journal of M e d ical Genetics with an updated bibliography on X-linked mental retardation (XIN?) and r e l a t e d subjects. W e did so last i n 1985. During t h e f i r s t 20 years of work i n the f i e l d (1944-1965) only a h l f dozen or sc papers were publ.ished on XIMK. The bibliography published by Turner and O p i t z [Am J Med Genet 7:407-4151 c i t e d sme 180 items; t h e Conference R e p o r t cjn +b.e ( F i r s t ) Iriternational Workshop on t h e f r a g i l e X and X-linked Mental Retardation by Opitz ~x-~d. Sutherland [Am J Med Genet 17:5-94, 19841 listed sore 360 items; m-d t h e (1985): A comparison of fragile X expression i n blood md lyqhoblastoid cultures. Am J Hum Genet 37:A84 (only) [Suppll. methior~ne and 5-azacytidine on fragile X expression. Am J Hum Genet 37:193-198.B r e w s t e r T, Moreau E , Wilson M, Brcanley W, R.derick T, L a t t SA (1984): A strategy t o reveal high-frequency k r u z z o MA, Mayer M, Jacobs FA (1985): ?'he effect of Aldridge J, K u n k e l L, B r u n s G, Tantravahi U, Lalande M, XLMR Bibliography 71 RFLPs along the human X chrmsame. Am J Hum Genet 36:546-564. Atkin JF, F l a i t z K, P a t i l S, Smith W (1985): A new X--linked m n t a l retardation s y n d r m . Am J Med Genet 21:697-705. Baraitser M, Burn J (1984): Brief clinical report: Neural tube defects a s an X-linked condition. Am J M e d Genet i7:m-385. Barbi G, Steinbach P, Baur S, Vogel W (1985): Manifestat i o n of the f r a g i l e site Xq27 i n fibroblasts. IV. Clones f r m a heterozygous f m l e do not marlifest this site hamogeneously on either the early o r late replicating X c h r m m . Confounding factors i n f r a g i l e X diagnosis -Possible e f f e c t s of medi.cations and smoking. Marrunalian C h r msome Newsletter 25:2 (only). factors i n f r a g i l e X diagnosis. (only) [Abstract]. Bartley JA, Miller DK, Hayford JT (1982): Concordance of X-linked glycerol kinase deficiency with X-linked cong e n i t a l adrenal h y p p l a s i a . Lancet 2:733-736. Beck M, Gl6ssl J, Fditer R, Kresse H (1983): Abnormal proteo dermatan s u l f a t e i n three patients with Coffin-Lmry syndrom. Pediatr R e s 17:926-928.

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