Rao KW - Search Results

1

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: rao kw. Am J Med Genet. 1990 Jul;36(3):306-9. doi: 10.1002/ajmg.1320360312. Am J Med Genet. 1990. PMID: 2363428

2

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: rao kw. 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.

3

Neurological aspects of del(1q) syndrome.

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

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: rao kw. 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: rao kw. Am J Med Genet. 1994 Jul 15;51(4):294-7. doi: 10.1002/ajmg.1320510403. Am J Med Genet. 1994. PMID: 7942990

6

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: rao kw. 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.

7

Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.

Estabrooks LL, Rao KW, Korf B. Estabrooks LL, et al. Among authors: rao kw. Am J Med Genet. 1993 Jan 1;45(1):97-100. doi: 10.1002/ajmg.1320450123. Am J Med Genet. 1993. PMID: 8418669

8

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: rao kw. Clin Genet. 1996 Apr;49(4):216-9. doi: 10.1111/j.1399-0004.1996.tb03290.x. Clin Genet. 1996. PMID: 8828989 Review.

9

A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

Estabrooks LL, Lamb AN, Kirkman HN, Callanan NP, Rao KW. Estabrooks LL, et al. Among authors: rao kw. Am J Hum Genet. 1992 Nov;51(5):971-8. Am J Hum Genet. 1992. PMID: 1384329 Free PMC article.

10

Autoimmune polyendocrinopathy associated with ring chromosome 18.

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

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