Lindenbaum RH - Search Results

1

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

Wilkie AO, Zeitlin HC, Lindenbaum RH, Buckle VJ, Fischel-Ghodsian N, Chui DH, Gardner-Medwin D, MacGillivray MH, Weatherall DJ, Higgs DR. Wilkie AO, et al. Among authors: lindenbaum rh. Am J Hum Genet. 1990 Jun;46(6):1127-40. Am J Hum Genet. 1990. PMID: 2339705 Free PMC article.

2

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Wilkie AO, Buckle VJ, Harris PC, Lamb J, Barton NJ, Reeders ST, Lindenbaum RH, Nicholls RD, Barrow M, Bethlenfalvay NC, et al. Wilkie AO, et al. Among authors: lindenbaum rh. Am J Hum Genet. 1990 Jun;46(6):1112-26. Am J Hum Genet. 1990. PMID: 2339704 Free PMC article.

3

Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.

Lamb J, Wilkie AO, Harris PC, Buckle VJ, Lindenbaum RH, Barton NJ, Reeders ST, Weatherall DJ, Higgs DR. Lamb J, et al. Among authors: lindenbaum rh. Lancet. 1989 Oct 7;2(8667):819-24. doi: 10.1016/s0140-6736(89)92995-4. Lancet. 1989. PMID: 2477654

4

Molecular studies of the fragile X syndrome.

Knight SJ, Hirst MC, Roche A, Christodoulou Z, Huson SM, Winter R, Fitchett M, McKinley MJ, Lindenbaum RH, Nakahori Y, et al. Knight SJ, et al. Among authors: lindenbaum rh. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):217-23. doi: 10.1002/ajmg.1320430135. Am J Med Genet. 1992. PMID: 1605194

5

Fraser syndrome (cryptophthalmos-syndactyly syndrome): a review of eleven cases with postmortem findings.

Boyd PA, Keeling JW, Lindenbaum RH. Boyd PA, et al. Among authors: lindenbaum rh. Am J Med Genet. 1988 Sep;31(1):159-68. doi: 10.1002/ajmg.1320310119. Am J Med Genet. 1988. PMID: 2851937

6

The FG syndrome: 7 new cases.

Thompson EM, Baraitser M, Lindenbaum RH, Zaidi ZH, Kroll JS. Thompson EM, et al. Among authors: lindenbaum rh. Clin Genet. 1985 Jun;27(6):582-94. doi: 10.1111/j.1399-0004.1985.tb02043.x. Clin Genet. 1985. PMID: 4017279

7

Pitted enamel hypoplasia in tuberous sclerosis patients and first-degree relatives.

Lygidakis NA, Lindenbaum RH. Lygidakis NA, et al. Among authors: lindenbaum rh. Clin Genet. 1987 Oct;32(4):216-21. doi: 10.1111/j.1399-0004.1987.tb03304.x. Clin Genet. 1987. PMID: 3677460

8

Maternal 3;13 chromosome insertion, with severe pre-eclampsia.

Boyd PA, Maher EJ, Lindenbaum RH, Hoogwerf AM, Redman C, Crocker M. Boyd PA, et al. Among authors: lindenbaum rh. Clin Genet. 1995 Jan;47(1):17-21. doi: 10.1111/j.1399-0004.1995.tb03915.x. Clin Genet. 1995. PMID: 7774038

9

Recurrence of neural tube defect in a group of at risk women: a 10 year study of Pregnavite Forte F.

Holmes-Siedle M, Lindenbaum RH, Galliard A. Holmes-Siedle M, et al. Among authors: lindenbaum rh. J Med Genet. 1992 Feb;29(2):134-5. doi: 10.1136/jmg.29.2.134. J Med Genet. 1992. PMID: 1613763 Free PMC article. No abstract available.

10

UK clinicians' knowledge of and attitudes to the prenatal diagnosis of single gene disorders.

Firth HV, Lindenbaum RH. Firth HV, et al. Among authors: lindenbaum rh. J Med Genet. 1992 Jan;29(1):20-3. doi: 10.1136/jmg.29.1.20. J Med Genet. 1992. PMID: 1532425 Free PMC article.

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