S. B. Fowlow

发表

Inverted duplication of 22pter----q11.21 in cat-eye syndrome.

C. Lin, J. Hoo, A. Robertson, 1986, American journal of medical genetics.

Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.

R. Weksberg, B. Williams, J. Squire, 1993, Human molecular genetics.

Autosomal recessive juvenile cataract in Hutterites.

R. Lowry, K. Morgan, W. Pearce, 1987, Ophthalmic paediatrics and genetics.

The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformities.

A. Hunter, R. Haslam, R. Lowry, 1979, American journal of medical genetics.

Screening for methylmalonic aciduria in Alberta: a voluntary program with particular significance for the Hutterite Brethren.

K. Morgan, S. B. Fowlow, T. M. Holmes, 1985, American journal of medical genetics.

Chromosome 6q deletions: a report of two additional cases and a review of the literature.

J. Hoo, A. Robertson, S. B. Fowlow, 1990, American journal of medical genetics.

A familial interstitial deletion of the long arm of chromosome 21

D. Hoar, A. Robertson, S. B. Fowlow, 1990, Clinical genetics.

Cytogenetic analysis of 400 sperm from three translocation heterozygotes

Renée H. Martin, S. B. Fowlow, K. Hildebrand, 1990, Human Genetics.

Multiple malformations and exposure to therapeutic ultrasound during organogenesis.

S. B. Fowlow, D. R. Mcleod, 1989, American journal of medical genetics.