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Items: 15

1.

Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia.

D'Angelo CS, Kohl I, Varela MC, de Castro CI, Kim CA, Bertola DR, Lourenço CM, Koiffmann CP.

Am J Med Genet A. 2010 Jan;152A(1):102-10. doi: 10.1002/ajmg.a.33160.

PMID:
20034100
2.

Monosomy 1p36 deletion syndrome.

Gajecka M, Mackay KL, Shaffer LG.

Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):346-56. Review.

PMID:
17918734
3.

A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.

Courtens W, Wauters J, Wojciechowski M, Reyniers E, Scheers S, van Luijk R, Rooms L, Kooy F, Wuyts W.

Clin Dysmorphol. 2007 Oct;16(4):231-9. Review.

PMID:
17786114
4.

Del 1p36 syndrome: a newly emerging clinical entity.

Battaglia A.

Brain Dev. 2005 Aug;27(5):358-61. Review.

PMID:
16023552
5.

Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.

Campeau PM, Ah Mew N, Cartier L, Mackay KL, Shaffer LG, Der Kaloustian VM, Thomas MA.

Am J Med Genet A. 2008 Dec 1;146A(23):3062-9. doi: 10.1002/ajmg.a.32563. Review.

PMID:
19006213
6.

Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances.

Daniel A, Baker E, Chia N, Haan E, Malafiej P, Hinton L, Clarke N, Adès L, Darmanian A, Callen D.

Am J Med Genet A. 2003 Feb 15;117A(1):57-64. Review.

PMID:
12548741
7.

Monosomy 1p36.

Slavotinek A, Shaffer LG, Shapira SK.

J Med Genet. 1999 Sep;36(9):657-63. Review.

8.

Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review.

Puvabanditsin S, Garrow E, Brandsma E, Savla J, Kunjumon B, Gadi I.

Am J Med Genet A. 2009 Aug;149A(8):1782-5. doi: 10.1002/ajmg.a.32972. Review.

PMID:
19610110
9.

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.

Goldstone AP.

Trends Endocrinol Metab. 2004 Jan-Feb;15(1):12-20. Review.

PMID:
14693421
10.

Subtelomeric 6p deletion: clinical, FISH, and array CGH characterization of two cases.

Le Caignec C, De Mas P, Vincent MC, Bocéno M, Bourrouillou G, Rival JM, David A.

Am J Med Genet A. 2005 Jan 15;132A(2):175-80. Review.

PMID:
15578619
11.

[An updated review of 1p36 deletion (monosomy) syndrome].

Bello S, Rodríguez-Moreno A.

Rev Chil Pediatr. 2016 Sep - Oct;87(5):411-421. doi: 10.1016/j.rchipe.2015.12.004. Epub 2016 Feb 12. Review. Spanish.

12.

Mini-Review: Monosomy 1p36 syndrome: reviewing the correlation between deletion sizes and phenotypes.

Rocha CF, Vasques RB, Santos SR, Paiva CL.

Genet Mol Res. 2016 Feb 22;15(1). doi: 10.4238/gmr.15017942. Review.

13.

1p36 deletion syndrome: an update.

Jordan VK, Zaveri HP, Scott DA.

Appl Clin Genet. 2015 Aug 27;8:189-200. doi: 10.2147/TACG.S65698. eCollection 2015. Review.

14.

1p36 Deletion Syndrome.

Battaglia A.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2008 Feb 1 [updated 2013 Jun 6].

15.

Dissecting hypertension by obesity identifies a locus at 1p36.

Morris BJ.

Hypertension. 2005 Dec;46(6):1256-8. Epub 2005 Oct 17. Review. No abstract available.

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