Aylsworth AS - Search Results

1

Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Estabrooks LL, Lamb AN, Aylsworth AS, Callanan NP, Rao KW. Estabrooks LL, et al. Among authors: aylsworth as. J Med Genet. 1994 Feb;31(2):103-7. doi: 10.1136/jmg.31.2.103. J Med Genet. 1994. PMID: 8182713 Free PMC article.

2

Neurological aspects of del(1q) syndrome.

Murayama K, Greenwood RS, Rao KW, Aylsworth AS. Murayama K, et al. Among authors: aylsworth as. Am J Med Genet. 1991 Sep 15;40(4):488-92. doi: 10.1002/ajmg.1320400424. Am J Med Genet. 1991. PMID: 1746617

3

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

Estabrooks LL, Rao KW, Donahue RP, Aylsworth AS. Estabrooks LL, et al. Among authors: aylsworth as. Am J Med Genet. 1990 Jul;36(3):306-9. doi: 10.1002/ajmg.1320360312. Am J Med Genet. 1990. PMID: 2363428

4

Preliminary phenotypic map of chromosome 4p16 based on 4p deletions.

Estabrooks LL, Rao KW, Driscoll DA, Crandall BF, Dean JC, Ikonen E, Korf B, Aylsworth AS. Estabrooks LL, et al. Among authors: aylsworth as. Am J Med Genet. 1995 Jul 17;57(4):581-6. doi: 10.1002/ajmg.1320570413. Am J Med Genet. 1995. PMID: 7573133

5

Fragile X phenotype in a patient with a large de novo deletion in Xq27-q28.

Albright SG, Lachiewicz AM, Tarleton JC, Rao KW, Schwartz CE, Richie R, Tennison MB, Aylsworth AS. Albright SG, et al. Among authors: aylsworth as. Am J Med Genet. 1994 Jul 15;51(4):294-7. doi: 10.1002/ajmg.1320510403. Am J Med Genet. 1994. PMID: 7942990

6

Multiple congenital malformations in an infant prenatally diagnosed with mosaicism for dup(lq) and del(Xq).

Wells SR, Kuller JA, Rao KW, Aylsworth AS. Wells SR, et al. Among authors: aylsworth as. Clin Genet. 1996 Apr;49(4):216-9. doi: 10.1111/j.1399-0004.1996.tb03290.x. Clin Genet. 1996. PMID: 8828989 Review.

7

Submicroscopic deletion 9(q34.3) and duplication 19(p13.3): identified by subtelomere specific FISH probes.

Quigley DI, Kaiser-Rogers K, Aylsworth AS, Rao KW. Quigley DI, et al. Among authors: aylsworth as. Am J Med Genet A. 2004 Feb 15;125A(1):67-72. doi: 10.1002/ajmg.a.20457. Am J Med Genet A. 2004. PMID: 14755469 Review.

8

Monozygotic twins discordant for partial trisomy 1.

Watson WJ, Katz VL, Albright SG, Rao KW, Aylsworth AS. Watson WJ, et al. Among authors: aylsworth as. Obstet Gynecol. 1990 Nov;76(5 Pt 2):949-51. Obstet Gynecol. 1990. PMID: 2216262

9

Autoimmune polyendocrinopathy associated with ring chromosome 18.

Jain N, Reitnauer PJ, Rao KW, Aylsworth AS, Calikoglu AS. Jain N, et al. Among authors: aylsworth as. J Pediatr Endocrinol Metab. 2011;24(9-10):847-50. doi: 10.1515/jpem.2011.320. J Pediatr Endocrinol Metab. 2011. PMID: 22145491

10

Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramnios.

Hansen WF, Bernard LE, Langlois S, Rao KW, Chescheir NC, Aylsworth AS, Smith DI, Robinson WP, Barrett IJ, Kalousek DK. Hansen WF, et al. Among authors: aylsworth as. Prenat Diagn. 1997 May;17(5):443-50. doi: 10.1002/(sici)1097-0223(199705)17:5<443::aid-pd82>3.0.co;2-2. Prenat Diagn. 1997. PMID: 9178319

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