Edwards M - Search Results

1

Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.

Wojcik MH, Srivastava S, Agrawal PB, Balci TB, Callewaert B, Calvo PL, Carli D, Caudle M, Colaiacovo S, Cross L, Demetriou K, Drazba K, Dutra-Clarke M, Edwards M, Genetti CA, Grange DK, Hickey SE, Isidor B, Küry S, Lachman HM, Lavillaureix A, Lyons MJ, Marcelis C, Marco EJ, Martinez-Agosto JA, Nowak C, Pizzol A, Planes M, Prijoles EJ, Riberi E, Rush ET, Russell BE, Sachdev R, Schmalz B, Shears D, Stevenson DA, Wilson K, Jansen S, de Vries BBA, Curry CJ. Wojcik MH, et al. Among authors: edwards m. Am J Med Genet A. 2023 Jul;191(7):1900-1910. doi: 10.1002/ajmg.a.63226. Epub 2023 May 14. Am J Med Genet A. 2023. PMID: 37183572 Free PMC article.

2

Hypertrichosis "cubiti" with facial asymmetry.

Edwards MJ, Crawford AE, Jammu V, Wise G. Edwards MJ, et al. Am J Med Genet. 1994 Oct 15;53(1):56-8. doi: 10.1002/ajmg.1320530112. Am J Med Genet. 1994. PMID: 7802037

3

Supernumerary ring chromosome 17 identified by fluorescent in situ hybridization.

Fagan K, Edwards M. Fagan K, et al. Among authors: edwards m. Am J Med Genet. 1997 Apr 14;69(4):352-5. Am J Med Genet. 1997. PMID: 9098481

4

Mixoploidy in humans: two surviving cases of diploid-tetraploid mixoploidy and comparison with diploid-triploid mixoploidy.

Edwards MJ, Park JP, Wurster-Hill DH, Graham JM Jr. Edwards MJ, et al. Am J Med Genet. 1994 Sep 1;52(3):324-30. doi: 10.1002/ajmg.1320520314. Am J Med Genet. 1994. PMID: 7810564

5

Scalp-ear-nipple syndrome: additional manifestations.

Edwards MJ, McDonald D, Moore P, Rae J. Edwards MJ, et al. Am J Med Genet. 1994 Apr 15;50(3):247-50. doi: 10.1002/ajmg.1320500307. Am J Med Genet. 1994. PMID: 8042668

6

Nevoid hypertrichosis with multiple patches of hair that underwent almost complete spontaneous resolution.

Dudding TE, Rogers M, Roddick LG, Relic J, Edwards MJ. Dudding TE, et al. Among authors: edwards mj. Am J Med Genet. 1998 Sep 23;79(3):195-6. doi: 10.1002/(sici)1096-8628(19980923)79:3<195::aid-ajmg8>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9788560 Review.

7

Esophageal dysmotility in brothers with an FG-like syndrome.

Smith RL, Edwards MJ, Notaras E, O'Loughlin EV. Smith RL, et al. Among authors: edwards mj. Am J Med Genet. 2000 Mar 20;91(3):185-9. Am J Med Genet. 2000. PMID: 10756339

8

X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males.

Edwards M, Mulcahy D, Turner G. Edwards M, et al. Clin Genet. 1988 Nov;34(5):325-32. doi: 10.1111/j.1399-0004.1988.tb02886.x. Clin Genet. 1988. PMID: 3229001

9

Herrmann multiple synostosis syndrome with neurological complications caused by spinal canal stenosis.

Edwards MJ, Rowe L, Petroff V. Edwards MJ, et al. Am J Med Genet. 2000 Nov 13;95(2):118-22. Am J Med Genet. 2000. PMID: 11078560

10

Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes.

Schnur RE, Wick PA, Bailey C, Rebbeck T, Weleber RG, Wagstaff J, Grix AW, Pagon RA, Hockey A, Edwards MJ. Schnur RE, et al. Among authors: edwards mj. Am J Hum Genet. 1994 Sep;55(3):484-96. Am J Hum Genet. 1994. PMID: 7915878 Free PMC article.

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