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Tijdschrift Voor Kindergeneeskunde|October 1, 1993

[Intrauterine invagination in a newborn infant]C W Zijlmans, F A Nabben

Tijdschrift Voor Kindergeneeskunde|April 1, 1988

[Problems of differential diagnosis in children with acute leukemia]K Hählen, F A Nabben, A J Veerman

Clinical Dysmorphology|April 1, 1997

Heminasal aplasia: a case report and review of the literature of the last 25 yearsA A van Kempen, F A Nabben, B C Hamel

Human Genetics|June 1, 1995

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyF A Hol, B C Hamel, M P Geurds, et al.

Clinical Genetics|October 1, 1983

Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibsW O Renier, F A Nabben, T W Hustinx, et al.

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Showing results (1-10 of 5) with videos related to

Sort By:

Pageof 1

Tijdschrift Voor Kindergeneeskunde|October 1, 1993

[Intrauterine invagination in a newborn infant]C W Zijlmans, F A Nabben

Tijdschrift Voor Kindergeneeskunde|April 1, 1988

[Problems of differential diagnosis in children with acute leukemia]K Hählen, F A Nabben, A J Veerman

Clinical Dysmorphology|April 1, 1997

Heminasal aplasia: a case report and review of the literature of the last 25 yearsA A van Kempen, F A Nabben, B C Hamel

Human Genetics|June 1, 1995

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation familyF A Hol, B C Hamel, M P Geurds, et al.

Clinical Genetics|October 1, 1983

Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibsW O Renier, F A Nabben, T W Hustinx, et al.

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