Winter RM - 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: winter rm. Am J Med Genet. 1988 Jan;29(1):107-15. doi: 10.1002/ajmg.1320290113. Am J Med Genet. 1988. PMID: 3344763

2

Moore-Federman syndrome and acromicric dysplasia: are they the same entity?

Winter RM, Patton MA, Challener J, Mueller RF, Baraitser M. Winter RM, et al. J Med Genet. 1989 May;26(5):320-5. doi: 10.1136/jmg.26.5.320. J Med Genet. 1989. PMID: 2732993 Free PMC article.

3

Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome.

Baraitser M, Winter RM. Baraitser M, et al. Among authors: winter rm. J Med Genet. 1988 Jan;25(1):41-3. doi: 10.1136/jmg.25.1.41. J Med Genet. 1988. PMID: 3351890 Free PMC article.

4

A recognisable short stature syndrome with premature aging and pigmented naevi.

Baraitser M, Insley J, Winter RM. Baraitser M, et al. Among authors: winter rm. J Med Genet. 1988 Jan;25(1):53-6. doi: 10.1136/jmg.25.1.53. J Med Genet. 1988. PMID: 3351893 Free PMC article.

5

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: winter rm. Am J Med Genet. 1987 Dec;28(4):965-70. doi: 10.1002/ajmg.1320280423. Am J Med Genet. 1987. PMID: 3688035

6

The 3-M syndrome.

Winter RM, Baraitser M, Grant DB, Preece MA, Hall CM. Winter RM, et al. J Med Genet. 1984 Apr;21(2):124-8. doi: 10.1136/jmg.21.2.124. J Med Genet. 1984. PMID: 6716411 Free PMC article.

7

Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.

Reardon W, Gibbons RJ, Winter RM, Baraitser M. Reardon W, et al. Among authors: winter rm. Am J Med Genet. 1995 Jan 30;55(3):285-7. doi: 10.1002/ajmg.1320550308. Am J Med Genet. 1995. PMID: 7726224

8

Mesomelic limb shortness: a previously unreported autosomal recessive type.

Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM. Reardon W, et al. Among authors: winter rm. Am J Med Genet. 1993 Oct 1;47(5):788-92. doi: 10.1002/ajmg.1320470537. Am J Med Genet. 1993. PMID: 8267013

9

Hemihypertrophy, hemimegalencephaly, and polydactyly.

Reardon W, Harding B, Winter RM, Baraitser M. Reardon W, et al. Among authors: winter rm. Am J Med Genet. 1996 Dec 11;66(2):144-9. doi: 10.1002/(SICI)1096-8628(19961211)66:2<144::AID-AJMG4>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8958320

10

Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'.

MacDermot KD, Winter RM, Taylor D, Baraitser M. MacDermot KD, et al. Among authors: winter rm. J Med Genet. 1991 Jan;28(1):18-26. doi: 10.1136/jmg.28.1.18. J Med Genet. 1991. PMID: 1999828 Free PMC article. Review.

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