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Clinical Genetics|November 17, 2007
Sex-linked deafnessM B Petersen, Q Wang, P J Willems
Clinical Genetics|May 3, 2006
Non-syndromic, autosomal-recessive deafnessM B Petersen, P J Willems
Clinical Genetics|May 11, 2007
Mitochondrial deafnessH Kokotas, M B Petersen, P J Willems
Human Genetics|May 1, 1996
Genetic deficiencies of the glycogen phosphorylase systemJ Hendrickx, P J Willems
Human Genetics|November 1, 1992
BglII RFLP in DXS 498 between the pigment gene repeat unit, RCP and GCPL Vits, P J Willems
Human Genetics|July 1, 1992
PCR detection of a BclI RFLP in the G6PD gene of CaucasiansP J Willems, L Vits
Prenatal Diagnosis|September 1, 1986
Rare chromosome 20 variants encountered during prenatal diagnosisM B Petersen
QRB. Quality Review Bulletin|June 1, 1989
Using patient satisfaction data: an ongoing dialogue to solicit feedbackM B Petersen
Clinical Genetics|July 19, 2002
Non-syndromic autosomal-dominant deafnessM B Petersen
Clinical Genetics|May 26, 2010
Genetic factors in non-syndromic congenital heart malformationsM W Wessels, P J Willems
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