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L J Sheffield

Showing results (21-30 of 61) with videos related to

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Prenatal Diagnosis|February 3, 2004
Screening approach for Fragile X syndromeM B Delatycki, L J Sheffield, S Wake, et al.
American Journal of Medical Genetics|June 1, 1991
Two forms of ring 13 in a child with rhabdomyosarcomaL E Voullaire, V Petrovic, L J Sheffield, et al.
American Journal of Medical Genetics|September 1, 1987
A genetic follow-up study of 64 patients with the Pierre Robin complexL J Sheffield, J A Reiss, K Strohm, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1993
An ultrasound renal cyst prevalence survey: specificity data for inherited renal cystic diseasesD Ravine, R N Gibson, J Donlan, et al.
American Journal of Medical Genetics|November 15, 1993
Limb deficiencies, chorion villus sampling, and advanced maternal ageJ Halliday, J Lumley, L J Sheffield, et al.
American Journal of Human Genetics|November 1, 1983
Regional localization for HLA by recombination with a fragile site at 6p23J C Mulley, J Hay, L J Sheffield, et al.
Australian and New Zealand Journal of Medicine|April 1, 1996
Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP)Z Rudzki, S E Rodgers, L J Sheffield, et al.
The Medical Journal of Australia|May 20, 1991
Perceptions of genetic risk in individuals with a one in two chance of developing autosomal dominant polycystic kidney diseaseD Ravine, L R McGregor, R G Walker, et al.
Clinical Dysmorphology|January 1, 1995
'Disorganization-like syndrome' with 47,XXY and unilateral narrowing of the common iliac arteryC G Woods, S Treleaven, F R Betheras, et al.
The Journal of Pediatrics|December 1, 1976
Chondrodysplasia punctata-23 cases of a mild and relatively common varietyL J Sheffield, D M Danks, V Mayne, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|February 3, 2004
Screening approach for Fragile X syndromeM B Delatycki, L J Sheffield, S Wake, et al.
American Journal of Medical Genetics|June 1, 1991
Two forms of ring 13 in a child with rhabdomyosarcomaL E Voullaire, V Petrovic, L J Sheffield, et al.
American Journal of Medical Genetics|September 1, 1987
A genetic follow-up study of 64 patients with the Pierre Robin complexL J Sheffield, J A Reiss, K Strohm, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 1993
An ultrasound renal cyst prevalence survey: specificity data for inherited renal cystic diseasesD Ravine, R N Gibson, J Donlan, et al.
American Journal of Medical Genetics|November 15, 1993
Limb deficiencies, chorion villus sampling, and advanced maternal ageJ Halliday, J Lumley, L J Sheffield, et al.
American Journal of Human Genetics|November 1, 1983
Regional localization for HLA by recombination with a fragile site at 6p23J C Mulley, J Hay, L J Sheffield, et al.
Australian and New Zealand Journal of Medicine|April 1, 1996
Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP)Z Rudzki, S E Rodgers, L J Sheffield, et al.
The Medical Journal of Australia|May 20, 1991
Perceptions of genetic risk in individuals with a one in two chance of developing autosomal dominant polycystic kidney diseaseD Ravine, L R McGregor, R G Walker, et al.
Clinical Dysmorphology|January 1, 1995
'Disorganization-like syndrome' with 47,XXY and unilateral narrowing of the common iliac arteryC G Woods, S Treleaven, F R Betheras, et al.
The Journal of Pediatrics|December 1, 1976
Chondrodysplasia punctata-23 cases of a mild and relatively common varietyL J Sheffield, D M Danks, V Mayne, et al.
Pageof 7