Bamforth JS - Search Results

1

Polytopic anomalies with agenesis of the lower vertebral column.

Bohring A, Lewin SO, Reynolds JF, Voigtländer T, Rittinger O, Carey JC, Köpernik M, Smith R, Zackai EH, Leonard NJ, Gritter HL, Bamforth JS, Okun N, McLeod DR, Super M, Powell P, Mundlos S, Hennekam RC, van Langen IM, Viskochil DH, Wiedemann HR, Opitz JM. Bohring A, et al. Among authors: bamforth js. Am J Med Genet. 1999 Nov 19;87(2):99-114. Am J Med Genet. 1999. PMID: 10533024 Review.

2

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome.

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG. Bamforth JS, et al. Am J Med Genet. 1989 Jan;32(1):93-9. doi: 10.1002/ajmg.1320320120. Am J Med Genet. 1989. PMID: 2650550

3

Lacrimo-auriculo-dento-digital syndrome: evidence for lower limb involvement and severe congenital renal anomalies.

Bamforth JS, Kaurah P. Bamforth JS, et al. Am J Med Genet. 1992 Aug 1;43(6):932-7. doi: 10.1002/ajmg.1320430605. Am J Med Genet. 1992. PMID: 1415342

4

Adams Oliver syndrome: a family with extreme variability in clinical expression.

Bamforth JS, Kaurah P, Byrne J, Ferreira P. Bamforth JS, et al. Am J Med Genet. 1994 Feb 15;49(4):393-6. doi: 10.1002/ajmg.1320490408. Am J Med Genet. 1994. PMID: 8160731

5

Amniotic band sequence: Streeter's hypothesis reexamined.

Bamforth JS. Bamforth JS. Am J Med Genet. 1992 Oct 1;44(3):280-7. doi: 10.1002/ajmg.1320440304. Am J Med Genet. 1992. PMID: 1488974 Review.

6

Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophy.

Kolski HK, Leonard NJ, Lemmers RJ, Bamforth JS. Kolski HK, et al. Among authors: bamforth js. Muscle Nerve. 2008 Apr;37(4):526-9. doi: 10.1002/mus.20941. Muscle Nerve. 2008. PMID: 18059038

7

Poland anomaly with a limb body wall disruption defect: case report and review.

Bamforth JS, Fabian C, Machin G, Honore L. Bamforth JS, et al. Am J Med Genet. 1992 Jul 15;43(5):780-4. doi: 10.1002/ajmg.1320430504. Am J Med Genet. 1992. PMID: 1642261 Review.

8

Genetic study of SOX9 in a case of campomelic dysplasia.

Giordano J, Prior HM, Bamforth JS, Walter MA. Giordano J, et al. Among authors: bamforth js. Am J Med Genet. 2001 Jan 15;98(2):176-81. doi: 10.1002/1096-8628(20010115)98:2<176::aid-ajmg1027>3.0.co;2-q. Am J Med Genet. 2001. PMID: 11223854

9

RE: An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study [Issekutz et al., 2005].

Lowry RB, Sibbald B, Bamforth JS. Lowry RB, et al. Among authors: bamforth js. Am J Med Genet A. 2005 Dec 1;139A(2):169; discussion 170-1. doi: 10.1002/ajmg.a.30992. Am J Med Genet A. 2005. PMID: 16278895 No abstract available.

10

Facial measurements in clinical genetics: How important are the instruments we use?

Shaner DJ, Peterson AE, Beattie OB, Bamforth JS. Shaner DJ, et al. Among authors: bamforth js. Am J Med Genet. 1998 Jun 5;77(5):384-90. doi: 10.1002/(sici)1096-8628(19980605)77:5<384::aid-ajmg6>3.0.co;2-n. Am J Med Genet. 1998. PMID: 9632167

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

47 results

Search Page

Filters