Morris MA - Search Results

1

De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features.

Makrythanasis P, Moix I, Gimelli S, Fluss J, Aliferis K, Antonarakis SE, Morris MA, Béna F, Bottani A. Makrythanasis P, et al. Among authors: morris ma. Clin Genet. 2010 Aug;78(2):175-80. doi: 10.1111/j.1399-0004.2010.01371.x. Epub 2010 Jan 5. Clin Genet. 2010. PMID: 20236124

2

MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother.

Dayer AG, Bottani A, Bouchardy I, Fluss J, Antonarakis SE, Haenggeli CA, Morris MA. Dayer AG, et al. Among authors: morris ma. Brain Dev. 2007 Jan;29(1):47-50. doi: 10.1016/j.braindev.2006.06.001. Epub 2006 Jul 17. Brain Dev. 2007. PMID: 16844334

3

Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?

Makrythanasis P, Gimelli S, Béna F, Dahoun S, Morris MA, Antonarakis SE, Bottani A. Makrythanasis P, et al. Among authors: morris ma. Eur J Med Genet. 2012 Jan;55(1):63-6. doi: 10.1016/j.ejmg.2011.11.001. Epub 2011 Nov 10. Eur J Med Genet. 2012. PMID: 22080113

4

MECP2 duplication syndrome in a patient from Cameroon.

Tekendo-Ngongang C, Dahoun S, Nguefack S, Moix I, Gimelli S, Zambo H, Morris MA, Sloan-Béna F, Wonkam A. Tekendo-Ngongang C, et al. Among authors: morris ma. Am J Med Genet A. 2020 Apr;182(4):619-622. doi: 10.1002/ajmg.a.61510. Epub 2020 Feb 13. Am J Med Genet A. 2020. PMID: 32052928 Free PMC article.

5

Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients.

Martinet D, Filges I, Besuchet Schmutz N, Morris MA, Gaide AC, Dahoun S, Bottani A, Addor MC, Antonarakis SE, Beckmann JS, Béna F. Martinet D, et al. Among authors: morris ma. Am J Med Genet A. 2008 Aug 15;146A(16):2094-102. doi: 10.1002/ajmg.a.32414. Am J Med Genet A. 2008. PMID: 18629875

6

Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter.

Chen H, Gos A, Morris MA, Antonarakis SE. Chen H, et al. Among authors: morris ma. Genomics. 1996 Aug 1;35(3):620-4. doi: 10.1006/geno.1996.0411. Genomics. 1996. PMID: 8812505

7

Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.

Eliez S, Morris MA, Dahoun-Hadorn S, DeLozier-Blanchet CD, Gos A, Sizonenko P, Antonarakis SE. Eliez S, et al. Among authors: morris ma. Am J Med Genet. 1997 Jun 13;70(3):222-8. doi: 10.1002/(sici)1096-8628(19970613)70:3<222::aid-ajmg3>3.0.co;2-y. Am J Med Genet. 1997. PMID: 9188657

8

A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y.

Chen H, Rossier C, Morris MA, Scott HS, Gos A, Bairoch A, Antonarakis SE. Chen H, et al. Among authors: morris ma. Hum Genet. 1999 Nov;105(5):399-409. doi: 10.1007/s004390051122. Hum Genet. 1999. PMID: 10598804

9

Mapping of the human transcription factor GABPA (E4TF1-60) gene to chromosome 21.

Chrast R, Chen H, Morris MA, Antonarakis SE. Chrast R, et al. Among authors: morris ma. Genomics. 1995 Jul 1;28(1):119-22. doi: 10.1006/geno.1995.1117. Genomics. 1995. PMID: 7590737

10

Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report.

Hamamy H, Antonarakis SE, Cavalli-Sforza LL, Temtamy S, Romeo G, Kate LP, Bennett RL, Shaw A, Megarbane A, van Duijn C, Bathija H, Fokstuen S, Engel E, Zlotogora J, Dermitzakis E, Bottani A, Dahoun S, Morris MA, Arsenault S, Aglan MS, Ajaz M, Alkalamchi A, Alnaqeb D, Alwasiyah MK, Anwer N, Awwad R, Bonnefin M, Corry P, Gwanmesia L, Karbani GA, Mostafavi M, Pippucci T, Ranza-Boscardin E, Reversade B, Sharif SM, Teeuw ME, Bittles AH. Hamamy H, et al. Among authors: morris ma. Genet Med. 2011 Sep;13(9):841-7. doi: 10.1097/GIM.0b013e318217477f. Genet Med. 2011. PMID: 21555946 Free article.

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