Baraitser M - Search Results

1

A familial syndrome of microcephaly, sparse hair, mental retardation, and seizures.

van Haeringen A, Hurst JA, Savidge R, Baraitser M. van Haeringen A, et al. Among authors: baraitser m. J Med Genet. 1990 Feb;27(2):127-9. doi: 10.1136/jmg.27.2.127. J Med Genet. 1990. PMID: 2319580 Free PMC article.

2

Hereditary neurocutaneous angiomatous malformations: autosomal dominant inheritance in two families.

Hurst J, Baraitser M. Hurst J, et al. Among authors: baraitser m. Clin Genet. 1988 Jan;33(1):44-8. doi: 10.1111/j.1399-0004.1988.tb04263.x. Clin Genet. 1988. PMID: 3342546

3

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

4

A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.

Hurst JA, Baraitser M, Winter RM. Hurst JA, et al. Among authors: baraitser m. Am J Med Genet. 1987 Dec;28(4):965-70. doi: 10.1002/ajmg.1320280423. Am J Med Genet. 1987. PMID: 3688035

5

Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalities.

Hurst JA, Baraitser M, Wonke B. Hurst JA, et al. Among authors: baraitser m. Am J Med Genet. 1991 Sep 15;40(4):482-4. doi: 10.1002/ajmg.1320400422. Am J Med Genet. 1991. PMID: 1746615

6

The Holt-Oram syndrome.

Hurst JA, Hall CM, Baraitser M. Hurst JA, et al. Among authors: baraitser m. J Med Genet. 1991 Jun;28(6):406-10. doi: 10.1136/jmg.28.6.406. J Med Genet. 1991. PMID: 1870097 Free PMC article. No abstract available.

7

Balanced t(6;8)(6p8p;6q8q) and the CHARGE association.

Hurst JA, Meinecke P, Baraitser M. Hurst JA, et al. Among authors: baraitser m. J Med Genet. 1991 Jan;28(1):54-5. doi: 10.1136/jmg.28.1.54. J Med Genet. 1991. PMID: 1999835 Free PMC article.

8

De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.

Temple IK, Hurst JA, Hing S, Butler L, Baraitser M. Temple IK, et al. Among authors: baraitser m. J Med Genet. 1990 Jan;27(1):56-8. doi: 10.1136/jmg.27.1.56. J Med Genet. 1990. PMID: 2308156 Free PMC article.

9

Johanson-Blizzard syndrome.

Hurst JA, Baraitser M. Hurst JA, et al. Among authors: baraitser m. J Med Genet. 1989 Jan;26(1):45-8. doi: 10.1136/jmg.26.1.45. J Med Genet. 1989. PMID: 2645405 Free PMC article. Review. No abstract available.

10

Microcephaly, mental retardation, cataracts, and hypogonadism in sibs: Martsolf's syndrome.

Harbord MG, Baraitser M, Wilson J. Harbord MG, et al. Among authors: baraitser m. J Med Genet. 1989 Jun;26(6):397-400. doi: 10.1136/jmg.26.6.397. J Med Genet. 1989. PMID: 2738902 Free PMC article.

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