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American Journal of Medical Genetics|October 1, 1993
Cerebral malformation, seizures, hypertrichosis, distinct face, claw hands, and overlapping fingers in sibs of both sexesF M Müller, G M Barth, H Menger, et al.
Molecular and Cellular Probes|June 1, 1996
Two different PAX3 gene mutations causing Waardenburg syndrome type IG Wildhardt, A Winterpacht, K Hilbert, et al.
Pediatric Radiology|January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasiaJ Spranger, H Menger, S Mundlos, et al.
Der Nervenarzt|June 1, 1993
[A rare differential diagnosis of waddling gait--osteomalacia caused by vitamin D deficiency]H Menger, H Pfingsten, G Hintze, et al.
American Journal of Medical Genetics|October 23, 1997
Vitamin K deficiency embryopathy: a phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolismH Menger, A E Lin, H V Toriello, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|May 13, 1998
[Does maternal obesity increase the risk of fetal abnormalities? Analysis of 20,248 newborn infants of the Mainz Birth Register for detecting congenital abnormalities]A Queisser-Luft, D Kieninger-Baum, H Menger, et al.
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