Nabben FA - Search Results

1

Localization of Alagille syndrome to 20p11.2-p12 by linkage analysis of a three-generation family.

Hol FA, Hamel BC, Geurds MP, Hansmann I, Nabben FA, Daniëls O, Mariman EC. Hol FA, et al. Among authors: nabben fa. Hum Genet. 1995 Jun;95(6):687-90. doi: 10.1007/BF00209488. Hum Genet. 1995. PMID: 7789956 Free article.

2

Heminasal aplasia: a case report and review of the literature of the last 25 years.

van Kempen AA, Nabben FA, Hamel BC. van Kempen AA, et al. Among authors: nabben fa. Clin Dysmorphol. 1997 Apr;6(2):147-52. Clin Dysmorphol. 1997. PMID: 9134295 Review.

3

Partial trisomy of chromosome 1 resulting from a complex maternal rearrangement of chromosomes 1, 5, and 6.

Hustinx TW, Nabben FA, Scheres JM. Hustinx TW, et al. Among authors: nabben fa. Am J Med Genet. 1979;3(4):353-8. doi: 10.1002/ajmg.1320030406. Am J Med Genet. 1979. PMID: 474635 No abstract available.

4

Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs.

Renier WO, Nabben FA, Hustinx TW, Veerkamp JH, Otten BJ, Ter Laak HJ, Ter Haar BG, Gabreëls FJ. Renier WO, et al. Among authors: nabben fa. Clin Genet. 1983 Oct;24(4):243-51. doi: 10.1111/j.1399-0004.1983.tb00078.x. Clin Genet. 1983. PMID: 6315281

5

HB Mizuho or alpha 2 beta 2 68(E12)Leu-->Pro in a young Dutch boy.

Harthoorn-Lasthuizen EJ, Nabben FA, Kazanetz EG, Gu LH, Molchanova TP, Huisman TH. Harthoorn-Lasthuizen EJ, et al. Among authors: nabben fa. Hemoglobin. 1995 May-Jul;19(3-4):203-6. doi: 10.3109/03630269509036941. Hemoglobin. 1995. PMID: 7558877 No abstract available.

6

[Hyperbilirubinemia in healthy full-term neonates: guidelines for diagnosis and treatment].

Nabben FA. Nabben FA. Ned Tijdschr Geneeskd. 1997 Mar 8;141(10):495-6. Ned Tijdschr Geneeskd. 1997. PMID: 9173296 Dutch. No abstract available.

7

[Intrauterine invagination in a newborn infant].

Zijlmans CW, Nabben FA. Zijlmans CW, et al. Among authors: nabben fa. Tijdschr Kindergeneeskd. 1993 Oct;61(5):191-4. Tijdschr Kindergeneeskd. 1993. PMID: 8266316 Dutch.

8

[Ultrasonography as initial imaging study can replace roentgen studies under certain conditions in suspected congenital hip dysplasia].

Nabben FA. Nabben FA. Ned Tijdschr Geneeskd. 1992 Jul 3;136(27):1318. Ned Tijdschr Geneeskd. 1992. PMID: 1630522 Dutch. No abstract available.

9

[Problems of differential diagnosis in children with acute leukemia].

Hählen K, Nabben FA, Veerman AJ. Hählen K, et al. Among authors: nabben fa. Tijdschr Kindergeneeskd. 1988 Apr;56(2):45-9. Tijdschr Kindergeneeskd. 1988. PMID: 3376093 Dutch.

10

[True hermaphroditism with a chromosome mosaic of XX-XY-XXY].

Broeders GH, van Hinsbergh WC, Kirkels VG, Nabben FA. Broeders GH, et al. Among authors: nabben fa. Ned Tijdschr Geneeskd. 1974 May 11;118(19):726-32. Ned Tijdschr Geneeskd. 1974. PMID: 4827216 Dutch. No abstract available.

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