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Developmental Medicine and Child Neurology|April 1, 1990
An extended family with a dominantly inherited speech disorderJ A Hurst, M Baraitser, E Auger, et al.Therapeutic Drug Monitoring|January 1, 1984
Falsely increased digoxin concentrations in samples from neonates and infantsJ M Hicks, E M BrettClinical Chemistry|June 1, 1981
A bioluminescence micromethod for measuring chloramphenicol in serumR L Boeckx, E M BrettClinical Chemistry|October 1, 1981
Total-calcium measurement in serum from neonates: limitations of current methodsE M Brett, J M HicksClinical Dysmorphology|May 8, 1998
Rapadilino syndrome--a non-Finnish caseS G Kant, M Baraitser, P J Milla, et al.Clinical Dysmorphology|April 1, 1997
Selective IgG2 subclass deficiency--a marker for the syndrome of pre/postnatal growth retardation, developmental delay, hypotrophy of distal extremities, dental anomalies and eczemaS B Ainsworth, M Baraitser, R F Mueller, et al.Journal of Medical Genetics|February 1, 1987
An oculocerebral hypopigmentation syndrome: a case report with clinical, histochemical, and ultrastructural findingsM A Patton, M Baraitser, A H Heagerty, et al.Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, et al.Prenatal Diagnosis|March 1, 1986
Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (Opitz-G syndrome)M A Patton, M Baraitser, K Nickolaides, et al.Journal of Medical Genetics|October 1, 1984
The femoral hypoplasia-unusual facies syndromeJ Burn, R M Winter, M Baraitser, et al.Pageof 19