Bibliotecas PUC-SP - Busca Integrada

"Code of practice and guidance on human genetic testing services supplied direct to the public". Advisory Committee on Genetic Testing.

af Barber, J C
Udgivet 1998

Comments on important genetic topics from papers in other journals: Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

af Barber, J C K
Udgivet 1992

Comments on important genetic topics from papers in other journals: Prospects for homologous recombination in human gene therapy

af Barber, J C K
Udgivet 1992

Medical genetics: advances in brief: Diagnosis of human genetic disease using recombinant DNA. Fourth edition

af Barber, J C K
Udgivet 1994

A de novo X;13 translocation with abnormal phenotype.

af Hodgson, S V, Barber, J C, Dowie, A, Dubowitz, V
Udgivet 1986

Diaphragmatic herniae and translocations involving 8q22 in two patients.

af Temple, I K, Barber, J C, James, R S, Burge, D
Udgivet 1994

Partial monosomy 3q in a boy with short stature, developmental delay, and mild dysmorphic features.

af Brueton, L A, Barber, J C, Huson, S M, Winter, R M
Udgivet 1989

Extensive Normal Copy Number Variation of a β-Defensin Antimicrobial-Gene Cluster

af Hollox, E. J., Armour, J. A. L., Barber, J. C. K.
Udgivet 2003

Fatal disseminated cryptococcosis following intraocular involvement.

af Schulman, J A, Leveque, C, Coats, M, Lawrence, L, Barber, J C
Udgivet 1988

Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients.

af Joyce, C A, Zorich, B, Pike, S J, Barber, J C, Dennis, N R
Udgivet 1996

Human fibroblast interferon in tears of patients with picornavirus epidemic conjunctivitis.

af Langford, M P, Yin-Murphy, M, Ho, Y M, Barber, J C, Baron, S, Stanton, G J
Udgivet 1980

Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations.

af Swerdlow, A. J., Jacobs, P. A., Marks, A., Maher, E. J., Young, T., Barber, J. C., Vaughan Hudson, G.
Udgivet 1996

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.

af Browne, C E, Dennis, N R, Maher, E, Long, F L, Nicholson, J C, Sillibourne, J, Barber, J C
Udgivet 1997

Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.

af Barber, J C, Ellis, K H, Bowles, L V, Delhanty, J D, Ede, R F, Male, B M, Eccles, D M
Udgivet 1994

RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.

af Power, M M, James, R S, Barber, J C, Fisher, A M, Wood, P J, Leatherdale, B A, Flanagan, D E, Hatchwell, E
Udgivet 1997

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.

af Flynn, G A, Hirst, M C, Knight, S J, Macpherson, J N, Barber, J C, Flannery, A V, Davies, K E, Buckle, V J
Udgivet 1993

Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

af Barber, J C, Joyce, C A, Collinson, M N, Nicholson, J C, Willatt, L R, Dyson, H M, Bateman, M S, Green, A J, Yates, J R, Dennis, N R
Udgivet 1998