Robertson SP - Search Results

1

Zimmermann-Laband syndrome in an adult. Long-term follow-up of a patient with vascular and cardiac complications.

Robertson SP, Lipp H, Bankier A. Robertson SP, et al. Am J Med Genet. 1998 Jun 30;78(2):160-4. doi: 10.1002/(sici)1096-8628(19980630)78:2<160::aid-ajmg12>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9674908

2

The 4q-syndrome: delineation of the minimal critical region to within band 4q31.

Robertson SP, O'Day K, Bankier A. Robertson SP, et al. Clin Genet. 1998 Jan;53(1):70-3. doi: 10.1034/j.1399-0004.1998.531530114.x. Clin Genet. 1998. PMID: 9550366

3

Sotos syndrome and cutis laxa.

Robertson SP, Bankier A. Robertson SP, et al. J Med Genet. 1999 Jan;36(1):51-6. J Med Genet. 1999. PMID: 9950366 Free PMC article.

4

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome.

Robertson SP, Kirk E, Bernier F, Brereton J, Turner A, Bankier A. Robertson SP, et al. Am J Med Genet. 1999 Aug 6;85(4):395-402. Am J Med Genet. 1999. PMID: 10398267

5

Oromandibular limb hypogenesis complex (Hanhart syndrome): a severe adult phenotype.

Robertson SP, Bankier A. Robertson SP, et al. Am J Med Genet. 1999 Apr 23;83(5):427-9. Am J Med Genet. 1999. PMID: 10232758 No abstract available.

6

Hypogonadotrophic hypogonadism in Roifman syndrome.

Robertson SP, Rodda C, Bankier A. Robertson SP, et al. Clin Genet. 2000 Jun;57(6):435-8. doi: 10.1034/j.1399-0004.2000.570606.x. Clin Genet. 2000. PMID: 10905663

7

An autosomal dominant or X-linked osteodysplastic disorder with severe cervical involvement.

Robertson SP, Dickens R, Savarirayan R, Rogers JG. Robertson SP, et al. Am J Med Genet. 1999 Mar 5;83(1):17-22. Am J Med Genet. 1999. PMID: 10076880 Review.

8

Are Melnick-Needles syndrome and oto-palato-digital syndrome type II allelic? Observations in a four-generation kindred.

Robertson S, Gunn T, Allen B, Chapman C, Becroft D. Robertson S, et al. Am J Med Genet. 1997 Aug 22;71(3):341-7. doi: 10.1002/(sici)1096-8628(19970822)71:3<341::aid-ajmg16>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9268106

9

Cerebral infarction in Noonan syndrome.

Robertson S, Tsang B, Aftimos S. Robertson S, et al. Am J Med Genet. 1997 Jul 11;71(1):111-4. doi: 10.1002/(sici)1096-8628(19970711)71:1<111::aid-ajmg20>3.0.co;2-o. Am J Med Genet. 1997. PMID: 9215779

10

FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited.

Adès LC, Sullivan K, Biggin A, Haan EA, Brett M, Holman KJ, Dixon J, Robertson S, Holmes AD, Rogers J, Bennetts B. Adès LC, et al. Am J Med Genet A. 2006 May 15;140(10):1047-58. doi: 10.1002/ajmg.a.31202. Am J Med Genet A. 2006. PMID: 16596670

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