Robertson SP - Search Results

1

Macrocephaly--cutis marmorata telangiectatica congenita: report of five patients and a review of the literature.

Robertson SP, Gattas M, Rogers M, Adès LC. Robertson SP, et al. Clin Dysmorphol. 2000 Jan;9(1):1-9. Clin Dysmorphol. 2000. PMID: 10649789 Review.

2

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

3

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

4

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.

5

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

6

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.

7

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

8

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

9

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

10

Cerebrospinal fluid shunts in the management of behavioural problems in Sanfilippo syndrome (MPS III).

Robertson SP, Klug GL, Rogers JG. Robertson SP, et al. Eur J Pediatr. 1998 Aug;157(8):653-5. doi: 10.1007/s004310050904. Eur J Pediatr. 1998. PMID: 9727849

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