Lindenbaum RH - Search Results

1

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

2

Severe limb abnormalities after chorion villus sampling at 56-66 days' gestation.

Firth HV, Boyd PA, Chamberlain P, MacKenzie IZ, Lindenbaum RH, Huson SM. Firth HV, et al. Among authors: lindenbaum rh. Lancet. 1991 Mar 30;337(8744):762-3. doi: 10.1016/0140-6736(91)91374-4. Lancet. 1991. PMID: 1672394

3

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

4

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.

5

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.

6

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.

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

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.

9

Limb abnormalities and chorion villus sampling.

Firth HV, Boyd PA, Chamberlain P, MacKenzie IZ, Lindenbaum RH, Huson SM. Firth HV, et al. Among authors: lindenbaum rh. Lancet. 1991 Jul 6;338(8758):51. doi: 10.1016/0140-6736(91)90036-o. Lancet. 1991. PMID: 1676098 No abstract available.

10

Molecular studies of trisomy 18.

Fisher JM, Harvey JF, Lindenbaum RH, Boyd PA, Jacobs PA. Fisher JM, et al. Among authors: lindenbaum rh. Am J Hum Genet. 1993 Jun;52(6):1139-44. Am J Hum Genet. 1993. PMID: 8503446 Free PMC article. Review.

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