THE VICISSITUDES OF CHANGEHUGHES H. E.EDUC. URBAN SOC. 1972, Vol 4, Num 4, pp 489-496Article

Contracting for clinical genetic services : the Welsh modelHUGHES, H. E; ALDERMAN, J. K; KRAWCZAK, M et al.Journal of medical genetics. 1998, Vol 35, Num 4, pp 309-313, issn 0022-2593Article

Twenty-four cases of the EEC syndrome : clinical presentation and managementBUSS, P. W; HUGHES, H. E; CLARKE, A et al.Journal of medical genetics. 1995, Vol 32, Num 9, pp 716-723, issn 0022-2593Article

Long-term alterations in brain function following cocaine administration during the preweanling periodDOW-EDWARDS, D. L; FREED-MALEN, L. A; HUGHES, H. E et al.Developmental brain research. 1993, Vol 72, Num 2, pp 309-313, issn 0165-3806Article

Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafnessREARDON, W; ROBERTS, S; PHELPS, P. D et al.American journal of medical genetics. 1992, Vol 44, Num 4, pp 513-517, issn 0148-7299Article

Interstital deletion, del(4) (q33q35.1), in a mother and two childrenCURTIS, M. A; SMITH, R. A; SIBERT, J et al.Journal of medical genetics. 1989, Vol 26, Num 10, pp 652-654, issn 0022-2593Article

Mutation in KCNQ1 that has both recessive and dominant characteristicsMURRAY, A; POTET, F; BELLOCQ, C et al.Journal of medical genetics. 2002, Vol 39, Num 9, pp 681-685, issn 0022-2593Article

Lateral meningocele syndrome : Three new patients and review of the literatureGRIPP, K. W; SCOTT, C. I; MILLER, F et al.American journal of medical genetics. 1997, Vol 70, Num 3, pp 229-239, issn 0148-7299Article

Coarctation of the aorta in Kabuki syndromeHUGHES, H. E; DAVIES, S. J.Archives of disease in childhood. 1994, Vol 70, Num 6, pp 512-514, issn 0003-9888Article

Very superior intelligence in a child with Noonan syndromeFINEGAN, J.-A. K; HUGHES, H. E.American journal of medical genetics. 1988, Vol 31, Num 2, pp 385-389, issn 0148-7299Article

German syndrome in sibsLEWIN, S. O; HUGHES, H. E.American journal of medical genetics. 1987, Vol 26, Num 2, pp 385-390, issn 0148-7299Article

Midtrimester amniocentesis: obstetric outcome and neonatal neurobehavioral statusFINEGAN, J.-A. K; QUARRINGTON, B. J; HUGHES, H. E et al.American journal of obstetrics and gynecology. 1984, Vol 150, Num 8, pp 989-997, issn 0002-9378Article

Costello syndrome : natural history and differential diagnosis of cutis laxaDAVIES, S. J; HUGHES, H. E.Journal of medical genetics. 1994, Vol 31, Num 6, pp 486-489, issn 0022-2593Article

Small cell lung carcinoma in a patient with sotos syndrome : are genes at 3p21 involved in both conditions ?COLE, T. R. P; HUGHES, H. E; JEFFREYS, M. J et al.Journal of medical genetics. 1992, Vol 29, Num 5, pp 338-341, issn 0022-2593Article

Bilateral split hand and split foot malformation in a boy withn a de novo interstitial deletion of 7q21.3ROBERTS, S. H; HUGHES, H. E; DAVIES, S. J et al.Journal of medical genetics. 1991, Vol 28, Num 7, pp 479-481, issn 0022-2593Article

Autosomal dominant macrocephaly : benign familial macrocephaly or a new syndrome ?COLE, T. R. P; HUGHES, H. E.American journal of medical genetics. 1991, Vol 41, Num 1, pp 115-124, issn 0148-7299Article

Child outcome following mid-trimester amniocentesis : development, behaviour, and physical status at age 4 yearsFINEGAN, J.-A. K; QUARRINGTON, B. J; HUGHES, H. E et al.British journal of obstetrics and gynaecology (Print). 1990, Vol 97, Num 1, pp 32-40, issn 0306-5456, 9 p.Article

Birth defects following maternal exposure to ergotamine, beta blockers, and caffeineHUGHES, H. E; GOLDSTEIN, D. A.Journal of medical genetics. 1988, Vol 25, Num 6, pp 396-399, issn 0022-2593Article

Congenital microcephaly due to vascular disruption: in utero documentationHUGHES, H. E; MISKIN, M.Pediatrics (Evanston). 1986, Vol 78, Num 1, pp 85-87, issn 0031-4005Article

Real-time epidemic forecasting for pandemic influenzaHALL, I. M; GANI, R; HUGHES, H. E et al.Epidemiology and infection. 2007, Vol 135, Num 3, pp 372-385, issn 0950-2688, 14 p.Article

Chromosome 2 interstitial deletion (del(2)(q14.1q21)) associated with connective tissue laxity and an attention deficit disorderBAKER, K. L; REES, M. I; THOMPSON, P. W et al.Journal of medical genetics. 2001, Vol 38, Num 7, pp 493-496, issn 0022-2593Article

Anal abnormalities in childhood myotonic dystrophy : a possible source of confusion in child sexual abuseREARDON, W; HUGHES, H. E; GREEN, S. H et al.Archives of disease in childhood. 1992, Vol 67, Num 4, pp 527-528, issn 0003-9888Article

The cardio-facio-cutaneous (CFC) syndrome and noonan syndrome : are they the same ?FRYER, A. E; HOLT, P. J; HUGHES, H. E et al.American journal of medical genetics. 1991, Vol 38, Num 4, pp 548-551, issn 0148-7299Article

α-thalassaemia/mental retardation syndrome (non-deletional type) : report of a family supporting X linked inheritanceCOLE, T. R. P; MAY, A; HUGHES, H. E et al.Journal of medical genetics. 1991, Vol 28, Num 11, pp 734-737, issn 0022-2593Article

Sotos syndromeCOLE, T. R. P; HUGHES, H. E.Journal of medical genetics. 1990, Vol 27, Num 9, pp 571-576, issn 0022-2593, 6 p.Article