A Doctor in PurgatoryBODURTHA J.Journal of the History of Medicine and Allied Sciences. 1976, Vol 31, Num 2, 215 p.Article

Magdalen HospitalBODURTHA, J.Journal of the History of Medicine and Allied Sciences New Haven, Conn. 1979, Vol 34, Num 3, 353 p.Article

Congenital central hypoventilation syndrome and Hirschsprung's disease in half sibsHAMILTON, J; BODURTHA, J. N.Journal of medical genetics. 1989, Vol 26, Num 4, pp 272-274, issn 0022-2593, 3 p.Article

Congenital hypopituitarism and microphthalmia. Report of two casesKAPLOWITZ, P. B; BODURTHA, J.Acta paediatrica (Oslo). 1993, Vol 82, Num 4, pp 419-422, issn 0803-5253Article

RHABDOMYOSARCOMA COMPLICATING MULTIPLE NEUROFIBROMATOSISMCKEEN EA; BODURTHA J; MEADOWS AT et al.1978; J. PEDIATR.; USA; DA. 1978; VOL. 93; NO 6; PP. 992-993; BIBL. 11 REF.Article

Nail size in normal infants: establishing standards for healthy term infantsSEABORG, B; BODURTHA, J.Clinical pediatrics. 1989, Vol 28, Num 3, pp 142-145, issn 0009-9228Article

Ethical considerations in oncology : balancing the interests of patients, oncologists, and societySMITH, T. J; BODURTHA, J. N.Journal of clinical oncology. 1995, Vol 13, Num 9, pp 2464-2470, issn 0732-183XArticle

Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10RAMPERSAUD, E; BASSUK, A. G; BODURTHA, J et al.Journal of medical genetics. 2005, Vol 42, Num 12, pp 940-946, issn 0022-2593, 7 p.Article

Ophthalmo-acromelic syndrome : Report and reviewTEKIN, M; TUTAR, E; ARSAN, S et al.American journal of medical genetics. 2000, Vol 90, Num 2, pp 150-154, issn 0148-7299Article

Seroepidemiology of cytomegalovirus and herpes simplex virus in twins and their familiesBODURTHA, J; ADLER, S. P; NANCE, W. E et al.American journal of epidemiology. 1988, Vol 128, Num 2, pp 268-276, issn 0002-9262Article

Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1PILZ, D. T; KUC, J; MATSUMOTO, N et al.Human molecular genetics (Print). 1999, Vol 8, Num 9, pp 1757-1760, issn 0964-6906Article

Partial trisomy 19p : case report and natural historySALBERT, B. A; SOLOMON, M; SPENCE, J. E et al.Clinical genetics. 1992, Vol 41, Num 3, pp 143-146, issn 0009-9163Article

F emoral duplication: a case reportBODURTHA, J; COUTINHO, M; BENATOR, R et al.American journal of medical genetics. 1989, Vol 33, Num 2, pp 165-169, issn 0148-7299Article

Goldenhar complex in discordant monozygotic twins: a case reort and review of the literatureBOLES, D. J; BODURTHA, J; NANCE, W. E et al.American journal of medical genetics. 1987, Vol 28, Num 1, pp 103-109, issn 0148-7299Article

Adrenal insufficiency after achalasia in the triple-A syndrome. EditorialPHILLIP, M; HERSHKOVITZ, E; SCHULMAN, H et al.Clinical pediatrics. 1996, Vol 35, Num 2, pp 99-102, issn 0009-9228Article

Arthritis, bleeding disorder and a chromosome marker ― A family studyATHREYA, B. H; BODURTHA, J; NICHOLS, W. W et al.Journal of rheumatology. 1987, Vol 14, Num 3, pp 535-539, issn 0315-162XArticle

Report of another family with Simpson-Golabi-Behme syndrome and a review of the literatureGARGANTA, C. L; BODURTHA, J. N.American journal of medical genetics. 1992, Vol 44, Num 2, pp 129-135, issn 0148-7299Article

Medical student elective in clinical geneticsBODURTHA, J; SPENCE, J. E; STEVENS, C. A et al.American journal of human genetics. 1991, Vol 49, Num 2, pp 494-496, issn 0002-9297Article

Analysis of variability of clinical manifestations in Waardenburg syndromeREYNOLDS, J. E; MEYER, J. M; LANDA, B et al.American journal of medical genetics. 1995, Vol 57, Num 4, pp 540-547, issn 0148-7299Article

Evidence for a major gene in familial anencephalySHAFFER, L. G; MARAZITA, M. L; BODURTHA, J et al.American journal of medical genetics. 1990, Vol 36, Num 1, pp 97-101, issn 0148-7299, 5 p.Article

Distinctive gastrointestinal anomaly associated with Coffin-Siris syndromeBODURTHA, J; KESSEL, A; BERMAN, W et al.The Journal of pediatrics. 1986, Vol 109, Num 6, pp 1015-1017, issn 0022-3476Article

Integrating genetic and genomic information into effective cancer care in diverse populationsFASHOYIN-AJE, L; SANGHAVI, K; BJORNARD, K et al.Annals of oncology. 2013, Vol 24, issn 0923-7534, vii48-vii54, SUP7Conference Paper

Progressive bilateral nasal alar collapse : a dominantly inherited traitCOLE, H; BODURTHA, J; SALBERT, B. A et al.American journal of medical genetics. 1992, Vol 42, Num 1, pp 88-89, issn 0148-7299Article

Monozygotic twins discordant for Ulrich-Turner syndromeKAPLOWITZ, P. B; BODURTHA, J; BROWN, J et al.American journal of medical genetics. 1991, Vol 41, Num 1, pp 78-82, issn 0148-7299Article

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformationsROSENBERG, M. J; KILLORAN, C; GRAHAM, J. M et al.Human genetics. 2001, Vol 109, Num 3, pp 311-318, issn 0340-6717Article