Baraitser M - Search Results

1

Distinctive syndrome of short stature, craniosynostosis, skeletal changes, and malformed ears.

Hurst JA, Winter RM, Baraitser M. Hurst JA, et al. Among authors: baraitser m. Am J Med Genet. 1988 Jan;29(1):107-15. doi: 10.1002/ajmg.1320290113. Am J Med Genet. 1988. PMID: 3344763

2

Genetics of Möbius syndrome.

Baraitser M. Baraitser M. J Med Genet. 1977 Dec;14(6):415-7. doi: 10.1136/jmg.14.6.415. J Med Genet. 1977. PMID: 604491 Free PMC article.

3

Joubert syndrome: a review.

Saraiva JM, Baraitser M. Saraiva JM, et al. Among authors: baraitser m. Am J Med Genet. 1992 Jul 1;43(4):726-31. doi: 10.1002/ajmg.1320430415. Am J Med Genet. 1992. PMID: 1341417 Review.

4

Neurological complications in one of a sibpair with aplasia cutis congenita.

Ho C, Baraitser M. Ho C, et al. Among authors: baraitser m. Clin Dysmorphol. 1992 Oct;1(4):235-9. Clin Dysmorphol. 1992. PMID: 1342876

5

Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour.

Grundy RG, Pritchard J, Baraitser M, Risdon A, Robards M. Grundy RG, et al. Among authors: baraitser m. Eur J Pediatr. 1992 Dec;151(12):895-8. doi: 10.1007/BF01954125. Eur J Pediatr. 1992. PMID: 1361910

6

Lethal congenital erythroderma: a newly recognised genetic disorder.

Shield JP, Judge MR, Reardon W, Baraitser M, Nohria M, Malone M, Harper JI. Shield JP, et al. Among authors: baraitser m. Clin Genet. 1992 May;41(5):273-7. doi: 10.1111/j.1399-0004.1992.tb03681.x. Clin Genet. 1992. PMID: 1535034

7

Distal spinal muscular atrophy with vocal cord paralysis.

Pridmore C, Baraitser M, Brett EM, Harding AE. Pridmore C, et al. Among authors: baraitser m. J Med Genet. 1992 Mar;29(3):197-9. doi: 10.1136/jmg.29.3.197. J Med Genet. 1992. PMID: 1552559 Free PMC article.

8

Genetic and clinical heterogeneity of Stickler syndrome.

Vintiner GM, Temple IK, Middleton-Price HR, Baraitser M, Malcolm S. Vintiner GM, et al. Among authors: baraitser m. Am J Med Genet. 1991 Oct 1;41(1):44-8. doi: 10.1002/ajmg.1320410113. Am J Med Genet. 1991. PMID: 1683158

9

Midline facial defects with ocular colobomata.

Temple IK, Brunner H, Jones B, Burn J, Baraitser M. Temple IK, et al. Among authors: baraitser m. Am J Med Genet. 1990 Sep;37(1):23-7. doi: 10.1002/ajmg.1320370107. Am J Med Genet. 1990. PMID: 1700608

10

Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotype.

Chitty LS, McCrimmon R, Temple IK, Russell-Eggitt IM, Baraitser M. Chitty LS, et al. Among authors: baraitser m. Am J Med Genet. 1991 Sep 15;40(4):417-20. doi: 10.1002/ajmg.1320400407. Am J Med Genet. 1991. PMID: 1746603 No abstract available.

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