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MARSHALL JD
LUDMAN MD
SHEA SE
SALISBURY SR
WILLI SM
LAROCHE RG
NISHINA PM
Citation: Jd. Marshall et al., GENEALOGY, NATURAL-HISTORY, AND PHENOTYPE OF ALSTROM-SYNDROME IN A LARGE ACADIAN KINDRED AND 3 ADDITIONAL FAMILIES, American journal of medical genetics, 73(2), 1997, pp. 150-161
Authors:
COULTERMACKIE MB
GAGNIER L
BEIS MJ
APPLEGARTH DA
COLE DEC
GORDON K
LUDMAN MD
Citation: Mb. Coultermackie et al., METACHROMATIC LEUKODYSTROPHY IN 3 FAMILIES FROM NOVA-SCOTIA, CANADA -A RECURRING MUTATION IN THE ARYLSULFATASE-A GENE, Journal of Medical Genetics, 34(6), 1997, pp. 493-498
Citation: Ct. Naugler et Md. Ludman, A CASE-CONTROL STUDY OF FLUCTUATING DERMATOGLYPHIC ASYMMETRY AS A RISK MARKER FOR DEVELOPMENTAL DELAY, American journal of medical genetics, 66(1), 1996, pp. 11-14
Citation: Ct. Naugler et Md. Ludman, FLUCTUATING ASYMMETRY AND DISORDERS OF DEVELOPMENTAL ORIGIN, American journal of medical genetics, 66(1), 1996, pp. 15-20
Citation: Ke. Gordon et al., SUCCESSFUL TREATMENT OF PAINFUL CRISES OF FABRY DISEASE WITH LOW-DOSEMORPHINE, Pediatric neurology, 12(3), 1995, pp. 250-251
Citation: Mb. Coultermackie et al., METACHROMATIC LEUKODYSTROPHY (MLD) IN A PATIENT WITH A CONSTITUTIONALRING CHROMOSOME-22, Journal of Medical Genetics, 32(10), 1995, pp. 787-791
Citation: Wl. Greer et al., LOCALIZING THE NIEMANN-PICK TYPE-II GENE (NOVA-SCOTIA VARIANT), American journal of human genetics, 57(4), 1995, pp. 1104-1104
Authors:
ENG CM
NIEHAUS DJ
ENRIQUEZ AL
BURGERT TS
LUDMAN MD
DESNICK RJ
Citation: Cm. Eng et al., FABRY-DISEASE - 23 MUTATIONS INCLUDING SENSE AND ANTISENSE CPG ALTERATIONS AND IDENTIFICATION OF A DELETIONAL HOT-SPOT IN THE ALPHA-GALACTOSIDASE-A GENE, Human molecular genetics, 3(10), 1994, pp. 1795-1799
Authors:
LUDMAN MD
VINCER MJ
CRON C
AGUIAR M
COHEN MM
Citation: Md. Ludman et al., HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS - ANOTHER CASE AND REVIEW, American journal of medical genetics, 47(3), 1993, pp. 352-356
Citation: F. Tremblay et al., LONGITUDINAL-STUDY OF THE EARLY ELECTRORETINOGRAPHIC CHANGES IN ALSTROMS SYNDROME, American journal of ophthalmology, 115(5), 1993, pp. 657-665