Publicatielijst

Publicaties  F.J. Los

Een jarenlange en uitgebreide ervaring van de auteur met de prenatale diagnostiek.

Los FJ, de Wolf BTHM, Huisjes HJ (1979). Raised maternal serum-Alpha-Fetoprotein levels and spontaneous fetomaternal transfusions. Lancet ii:1210-1212.

Los FJ, Hagenaars AM, Huisjes HJ, de Bruyn HWA, Ruitenberg EJ (1980). Preventief onderzoek van zwangeren op defecten van de neurale buis van de foetus door bepaling van het gehalte aan α-foetoproteine in het serum. Ned Tijdschr Geneeskd 124: 1096-1101.

Los FJ (1980). Serum-AFP-screening van zwangeren op foetale neuraalbuisdefekten. Groningen: proefschrift.

Hagenaars AM, Nagel J, Ruitenberg EJ, de Bruyn HWA, Huisjes HJ, Los FJ, van Knapen F, Menke HE, Oosterom J (1981). Toepasbaarheid van de Enzyme Linked Immunosorbent Assay (ELISA) ten behoeve van het routine onderzoek bij zwangeren naar het voorkomen van een aantal infectieziekten en congenitale misvormingen. Rapport 157609001. Bilthoven: Rijksinstituut voor de Volksgezondheid.

Willems PJ, de Vries-van der Weerd S, Los FJ, Mandema E, Smit GPA (1984). Short-limbed dwarfism, subluxation of the knees, hypogenitalism, and dysmorphic facies: a new syndrome? J Clin Dysmorphol 2: 19-23.

Los FJ, de Bruyn HWA, van Beek Calkoen-Carpay T, Huisjes HJ (1985). AFP transport across the fetal membranes in the human. Prenat Diagn 5: 277-281.

Boersma ER, Los FJ, Offringa PJ (1987). Infectious gastro-enteritis in children, patho-physiology and management. In: Van der Waay D & Saleh AEC (Eds) The Jonxis lectures: postgraduate course on infectious diseases, Curaçao, 1985: 53-70.

Beishuizen A, Derksen-Lubsen G, Los F, Rothbarth Ph H, Sinaasappel M (1989). Een zuigeling met AIDS. Ned Tijdschr Geneeskd 133: 123-126.

Kleijer WJ, Hussaarts-Odijk LM, Los FJ, Pijpers L, de Bree PK, Duran M (1989). Prenatal diagnosis of purine nucleoside phosphorylase deficiency in the first and second trimester of pregnancy. Prenat Diagn 9: 401-407.

Los FJ, Pijpers L, Jahoda MGJ, Sachs ES, Reuss A, Hagenaars A, Wladimiroff JW (1989) Transabdominal chorionic villus sampling in the second trimester of pregnancy: feto-maternal transfusions in relation to pregnancy outcome. Prenat Diagn 9: 521-526.

Jahoda MGJ, Pijpers L, Reuss A, Los FJ, Wladimiroff JW, Sachs ES (1989). Evaluation of transcervical chorionic villus sampling with a completed follow-up of 1550 consecutive pregnancies. Prenat Diagn 9: 621-628.

Halley DJJ, van Damme NHM, Deelen WH, Oostra BA, Jahoda MGJ, Sachs ES, Los FJ, Niermeijer MF (1989). Prenatal detection of major cystic fibrosis mutation. Lancet ii: 972.

Reuss A, den Hollander JC, Niermeijer MF, Wladimiroff JW, van Diggelen OP, Lindhout D, Los FJ (1989). Prenatal diagnosis of cystic kidney disease with ventriculomegaly: a report of six cases in two related sibships. Am J Med Genet 33: 385-389.

Pijpers L, Jahoda MGJ, Reuss A, Sachs ES, Los FJ, Wladimiroff JW (1989). Selective birth in a dizygotic twin pregnancy with discordancy for Down’s syndrome. Fetal Ther 4: 58-60.

Jahoda MGJ, Pijpers L, Reuss A, Brandenburg H, Cohen-Overbeek TE, Los FJ, Sachs ES, Wladimiroff JW (1990). Transabdominal villus sampling in early second trimester: a safe sampling method for women of advanced age. Prenat Diagn 10: 307-311.

Pijpers L, Kleijer WJ, Reuss A, Jahoda MGJ, Los FJ, Sachs ES, Wladimiroff JW (1990). Transabdominal chorionic villus sampling in a multiple pregnancy at risk of argininosuccinic aciduria: a case report. Am J Med Genet 36: 449-450.

Sachs ES, Jahoda MGJ, Los FJ, Pijpers L, Reuss A, Wladimiroff JW (1990). Interpretation of chromosome mosaicism and discrepancies in chorionic villi studies. Am J Med Genet 37: 268-271.

Brandenburg H, Jahoda MGJ, Wladimiroff JW, Los FJ, Lindhout D (1990). Convulsions in epileptic women after administration of prostaglandin E2 derivative. Lancet 336: 1138.

Sachs ES, Jahoda MGJ, Los FJ, Pijpers L, Wladimiroff JW (1990). Trisomy 21 mosaicism in gonads with unexpectedly high recurrence risks. Am J Med Genet 37 , Suppl 2: 186-188.

Frets PG, Los FJ, Sachs ES, Jahoda MGJ (1990). Psychological counseling of couples experiencing a pregnancy termination after amniocentsesis. J Psychosom Obstet Gynecol 11, Special Issue 1: 53-59.

Jahoda MGJ, Brandenburg H, Reuss A, Cohen-Overbeek TE, Wladimiroff JW, Los FJ, Sachs ES (1991). Transcervical (TC) and transabdominal (TA) CVS for prenatal diagnosis in Rotterdam: experience with 3611 cases. Prenat Diagn 11: 559-561.

Brandenburg H, Jahoda MGJ, Los FJ, Wladimiroff JW (1991). Acceptance of chorionic villus sampling in the southwest region of The Netherlands: a 5-year evaluation. Am J Med Genet 41: 236-238.

Sachs ES, Van Hemel JO, Los FJ (1992). Prenatal cytogenetic and postnatal molecular studies on 46,XX male. Lancet 339: 181-182.

Los FJ, Beekhuis JR, Marrink J, Hagenaars AM, Reuss A, Sachs ES, Jahoda MGJ, Wladimiroff JW (1992). Origin of raised maternal serum Alpha-Fetoprotein levels in second-trimester oligohydramnios. Prenat Diagn 12: 39-45.

Omtzigt JGC, Los FJ, Grobbee DE, Pijpers L, Jahoda MGJ, Brandenburg H, Stewart PA, Gaillard JLJ, Sachs ES, Wladimiroff JW, Lindhout D (1992). The risk of spina bifida aperta after first-trimester exposure to valproate in a prenatal cohort. Neurology 42, suppl 5: 119-125.

Los FJ, Hagenaars AM, Marrink J, Cohen-Overbeek TE, Gaillard JLJ, Brandenburg H (1992). Maternal serum Alpha-Fetoprotein levels and fetal outcome in early second-trimester oligohydramnios. Prenat Diagn 12: 285-292.

Smeets HJM, Nillesen WM, Los FJ, Busch HFM, Korneluk RG, Wieringa B, Brunner HG (1992). Prenatal diagnosis of myotonic dystrophy by direct mutation analysis. Lancet 340: 237-238.

De Winter JM, Janse HC, van Diggelen OP, Los FJ, Beemer FA, Kleijer WJ (1992). Prenatal diagnosis of Niemann-Pick disease type C. Clin Chim Acta 208: 173-181.

Kleijer WJ, Geilen GC, van Diggelen OP, Wevers R, Los FJ (1992). Prenatal analyses in a pregnancy at risk for β-mannosidosis. Prenat Diagn 12: 841-843.

Omtzigt JGC, Nau H, Los FJ, Pijpers L, Lindhout D (1992). The disposition of valproate and its metabolites in the late first trimester and early second trimester of pregnancy in maternal serum, urine, and amniotic fluid: effect of dose, co-medication, and the presence of spina bifida. Eur J Clin Pharmacol 43: 381-388.

Omtzigt JGC, Los FJ, Hagenaars AM, Stewart PA, Sachs ES, Lindhout D (1992). Prenatal diagnosis of spina bifida aperta after first-trimester valproate exposure exposure. Prenat Diagn 12: 893-897.

Heydanus R, Stewart PA, Wladimiroff JW, Los FJ (1993). Prenatal diagnosis of congenital cystic adenomatoid lung malformation: a report of seven cases. Prenat Diagn 13: 65-71.

Omtzigt JGC, Los FJ, Meijer JWA, Lindhout D (1993). The 10,11-epoxide-10,11-diol pathway of Carbamazepine in early pregnancy in maternal serum, urine, and amniotic fluid: effect of dose, comedication, and relation to outcome of pregnancy. Ther Drug Monitor 15: 1-10.

Jahoda MGJ, Brandenburg H, Cohen-Overbeek TE, Los FJ, Sachs ES, Wladimiroff JW (1993). Terminal transverse limb defects and early chorionic villus sampling: evaluation of 4,300 cases with completed follow-up. Am J Med Genet 46: 483-485.

Los FJ, Hagenaars AM, Jahoda MGJ, Wladimiroff JW, Brezinka Chr (1993). Fetal exsanguination by chorionic villus sampling. Lancet 342: 1559.

Los FJ, Van Hemel JO, Jacobs HJJ, Drop SLS, van Dongen JJM (1994). De novo deletion (2) (p11.2p13): clinical, cytogenetic, and immunological data. J Med Genet 31: 72-73.

Los FJ, van den Berg CDF, Braat A, in‘t Veld PA, Cohen-Overbeek TE, Jahoda MGJ (1994). Chromosomale afwijkingen bij de foetus met vroeg echografisch vastgesteld hygroma colli. Ned Tijdschr Obstet Gynaecol 107: 137.

Den Hollander NS, Cohen-Overbeek TE, Heydanus R, Stewart PA, Brandenburg H, Los FJ, Jahoda MGJ, Wladimiroff JW (1994). Cordocentesis for rapid karyotyping in fetuses with congenital anomalies or severe IUGR. Eur J Obstet Gynecol Reprod Biol 53: 183-187.

Los FJ, Hagenaars AM, Cohen-Overbeek TE, Quartero HWP (1994). Maternal serum markers in second-trimester oligohydramnios. Prenat Diagn 14: 565-568.

Kleijer WJ, van der Kraan M, Los FJ, Jaspers NGJ (1994). Prenatal diagnosis of ataxia-telangiectasia and Nijmegen Breakage Syndrome by the assay of radioresistant DNA synthesis. Int J Radiat Biol 66: S167-S174.

Van Opstal D, van den Berg C, Jahoda MGJ, Brandenburg H, Los FJ, in‘t Veld PA (1995). Retrospective study of trisomy 18 in chorionic villi with fluorescent in situ hybridization on archival direct preparations. Prenat Diagn 15: 51-55.

Los FJ, Janse HC, Brandenburg H, de Vrij RW, de Bruijn HWA (1995). Concanavalin A variants of Alpha-Fetoprotein in first trimester fetuses with trisomy 21 and with normal karyotypes. Gynecol Obstet Invest 39: 149-152.

Brandenburg H, Cohen-Overbeek TE, Los FJ, Jahoda MGJ (1995). Transabdominal chorionic villus sampling and bowel loops as a restricting factor. Prenat Diagn 15: 387-388.

Van den Ouweland AMW, van der Est M, Wesby-van Swaay E, Tijmensen TSLN, Los FJ, Van Hemel JO, Hennekam RCM, Meijers-Heijboer EJ, Niermeijer MF, Halley DJJ (1995). DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63). Hum Genet 95: 562-567.

Wladimiroff JW, Bhaggoe WR, Kristelijn M, Cohen-Overbeek TE, den Hollander NS, Los FJ (1995). Sonographically determined anomalies and outcome in 170 chromosomally abnormal fetuses. Prenat Diagn 15: 431-438.

Brezinka Chr, Hagenaars AM, Wladimiroff JW, Los FJ (1995). Fetal ductus venosus flow velocity waveforms and maternal serum AFP before and after first-trimester transabdominal chorionic villus sampling. Prenat Diagn 15: 699-703.

Van Opstal D, Van Hemel JO, Eussen BHJ, van der Heide A, van den Berg C, in‘t Veld PA, Los FJ (1995). A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei. Prenat Diag 15: 705-711.

In‘t Veld PA, Brandenburg H, Verhoeff A, Dhont M, Los FJ (1995). Sex chromosomal abnormalities and intra-cytoplasmatic sperm injection. Lancet 346: 773.

In’t Veld PA, Van Opstal D, van den Berg C, van Ooijen M, Brandenburg H, Pijpers L, Jahoda MGJ, Stijnen Th, Los FJ (1995). Increased incidence of cytogenetic abnormalities in chorionic villus samples from pregnancies established by in vitro fertilization and embryo transfer (IVF-ET). Prenat Diagn 15: 975-980.

Los FJ, Van Opstal D, Schol MP, Gaillard JLJ, Brandenburg H, van den Ouweland AMW, in’t Veld PA (1995). Prenatal diagnosis of mosaic tetrasomy 12p by fluorescent in situ hybridization in amniotic fluid cells: a case report of Pallister-Killian syndrome. Prenat Diagn 15: 1155-1159.

Frets PG, Los FJ, Brandenburg H, Niermeijer MF (1995). Gewenst en toch afgebroken….. Tijdschrift voor Verloskundigen 12: 554-559.

Brandenburg H, Los FJ, Cohen-Overbeek TE (1996). A case of early intrauterine Parvovirus B19 infection. Prenat Diagn 16: 75-77.

Brandenburg H, Los FJ, in’t Veld PA (1996). Clinical significance of placental-confined nonmosaic trisomy 16. Am J Obstet Gynecol 174: 1663-1664.

Los FJ, Noomen P, Vermeij-Keers Chr, Gaillard JLJ, Brandenburg H, Jahoda MGJ, Luider ThM (1996). Chorionic villus sampling and materno-fetal transfusions: an immunological pathogenesis of vascular disruptive syndromes? Prenat Diagn 16: 193-198.

Heydanus R, Raats MAM, Tibboel D, Los FJ, Wladimiroff JW (1996). Prenatal diagnosis of fetal abdominal wall defects: a retrospective analysis of 44 cases. Prenat Diagn 16: 411-417.

Cha’ban FK, van Splunder P, Los FJ, Wladimiroff JW (1996). Fetal outcome in nuchal translucency with emphasis on normal fetal karyotype. Prenat Diagn 16: 537-541.

Willemsen R, Oosterwijk JC, Los FJ, Galjaard H, Oostra BA (1996). Prenatal diagnosis of fragile X syndrome. Lancet 348: 967-968.

Los FJ, van den Berg C, Braat APG, Cha’ban FK, Kros JM, Van Opstal D (1996). Ring chromosome 18 in a fetus with only facial anomalies. Am J Med Genet 66: 216-220.

Luisterburg AJM, van der Zee DC, Gaillard JLJ, Los FJ, Brandenburg H, van Haeringen A, Vermeij-Keers Chr (1997). Chorionic villus sampling and end-artery disruption of the fetus. Prenat Diagn 17: 71-76.

Willemsen R, Los FJ, Mohkamsing S, van den Ouweland AMW, Deelen WH, Galjaard H, Oostra BA (1997). Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: a new appraisal. J Med Genet 34: 250-251.

Van Opstal D, Los FJ, Ramlakhan S, Van Hemel JO, van den Ouweland AMW, Brandenburg H, Pieters MHEC, Verhoeff A, Vermeer MCS, Dhont M, in’t Veld PA (1997). Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmatic sperm injection. Hum Reprod 12: 682-686.

In’t Veld PA, Weber RFA, Los FJ, den Hollander NS, Dhont M, Pieters MHEC, Van Hemel JO (1997). Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmatic sperm injection. Hum Reprod 12: 1642-1644.

Van den Berg C, Ramlakhan SK, Van Opstal D, Brandenburg H, Halley DJJ, Los FJ (1997). Prenatal diagnosis of trisomy 9: cytogenetic, FISH, and DNA studies. Prenat Diagn 17: 933-940.

Niermeijer MF, Los FJ, Brandenburg H (1997). Indicaties voor prenatale diagnostiek. In: Brandenburg H (Ed) Prenatale Diagnostiek. Houten/Diegem: Bohn, Stafleu & van Loghum: 1-9.

Los FJ, in’t Veld PA (1997). Cytogenetisch onderzoek in vlokken en vruchtwater. In: Brandenburg H (Ed) Prenatale Diagnostiek. Houten/Diegem: Bohn, Stafleu & van Loghum: 32-51.

Niermeijer MF, Los FJ (1997). Informing parents about the carrier status of their fetus. Am J Med Genet 73: 489.

Van Opstal D, van den Berg C, Deelen WH, Brandenburg H, Cohen-Overbeek TE, Halley DJJ, van den Ouweland AMW, in’t Veld PA, Los FJ (1998). Prospective prenatal investigations on potential uniparental disomy in cases of confined placental trisomy. Prenat Diagn 18: 35-44.

Niermeijer MF, Los FJ, Govaerts LCP, Van Hemel JO, Wouters CH (1998). Uitdragen van een zwangerschap bij een foetale prognose “infaust”. Ned Tijdschr Geneeskd 142: 485.

Los FJ, Van Opstal D, van den Berg C, Braat APG, Verhoef S, Wesby-van Swaay E, van den Ouweland AMW, Halley DJJ (1998). Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescue. Prenat Diagn 18: 659-668.

Los FJ, van den Berg C, Van Opstal D, Noomen P, Braat APG, Galjaard RJH, Pijpers L, Cohen-Overbeek TE, Wildschut HIJ, Brandenburg H (1998). Abnormal karyotypes in semi-direct chorionic villus preparations of women with different cytogenetic risks. Prenat Diagn 18: 1023-1040.

Los FJ, Brandenburg H, Niermeijer MF (1999). Vascular disruptive syndromes after exposure to misoprostol or chorionic villus sampling. Lancet 353: 843-844.

Van den Berg C, Braat APG, Van Opstal D, Halley DJJ, Kleijer WJ, den Hollander NS, Brandenburg H, Pijpers L, Los FJ (1999). Amniocentesis or chorionic villus sampling in multiple gestations? Experience with 500 cases. Prenat Diagn 19: 234-244.

Van den Berg C, Pijpers L, Halley DJJ, Van Opstal D, Los FJ (1999). Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation. Am J Med Genet 86: 151-155.

Los FJ, Van Opstal D (1999). False-negative findings in chorionic villi. Prenat Diagn 19: 891.

Van Opstal D, van den Berg C, Galjaard RJ, Los FJ (1999). Snelle prenatale diagnostiek in vruchtwater met behulp van fluorescentie in situ hybridisatie. Ned Tijdschr Obstet Gynaecol 112: 281-284.

Los FJ, van den Berg C, Galjaard RJH, Van Opstal D (1999). Vruchtwaterpunctie of vlokkentest? Ned Tijdschr Obstet Gynaecol 112: 285-288.

Beverstock GC, Mollevanger P, Baaij M, Lind J, van Ieperen L, Bartelings MM, Teunissen K, Brandenburg H, Van Opstal D, Los FJ (1999). Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis: a case report and review of the literature. Cancer Genet Cytogenet 115: 11-18.

Kleijer WJ, Geilen GC, Garritsen V, Huijmans JGM, Los FJ, Voznyi YV, van Diggelen OP (2000). First-trimester diagnosis of Morquio disease type A. Prenat Diagn 20: 183-185.

Den Hollander NS, Wessels MW, Los FJ, Ursem NTC, Niermeijer MF, Wladimiroff JW (2000). Congenital microcephaly detected by prenatal ultrasound: genetic aspects and clinical significance. Ultrasound Obstet Gynecol 15: 282-287.

Van den Berg C, Van Opstal D, Brandenburg H, Los FJ (2000). Case of 45,X/46,XY mosaicism with non-mosaic discordance between short-term villi (45,X) and cultured villi (46,XY). Am J Med Genet 93: 230-233.

Den Hollander NS, Kleijer WJ, Schoonderwaldt EM, Los FJ, Wladimiroff JW, Niermeijer MF (2000). In-utero diagnosis of mucopolysaccharidosis type VII in a fetus with an enlarged nuchal translucency. Ultrasound Obstet Gynecol 16: 87-90.

Van den Berg C, Van Opstal D, Brandenburg H, Wildschut HIJ, den Hollander NS, Pijpers L, Galjaard RJH, Los FJ (2000). Accuracy of abnormal karyotypes after the analysis of both short- and long-term culture of chorionic villi. Prenat Diagn 20: 956-969.

Van Opstal D, van den Berg C, Galjaard RJH, Los FJ (2001). Follow-up investigations in uncultured amniotic fluid cells after uncertain cytogenetic results. Prenat Diagn 21: 75-80.

Kleijer WJ, van Diggelen OP, Keulemans JLM, Losekoot M, Garritsen VH, Stroink H, Majoor-Krakauer D, Franken PF, Eurlings MCM, Taschner PEM, Los FJ, Galjaard RJH (2001). First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis. Prenat Diagn 21: 99-101.

Noomen P, van den Berg C, de Ruyter JLM, Van Opstal D, Los FJ (2001). Prevalence of tetraploid metaphases in semidirect and cultured chorionic villi. Fetal Diagn Ther 16: 129-132.

Vinkesteijn ASM, Jansen CLR, Los FJ, Mulder PGH, Wladimiroff JW (2001). Fetal transcerebellar diameter and chromosomal abnormalities. Ultrasound Obstet Gynecol 17: 502-505.

Van Haelst MM, Van Opstal D, Lindhout D, Los FJ (2001). Management of prenatally detected trisomy 8 mosaicism. Prenat Diagn 21: 1075-1078.

Los FJ, van den Berg C, Wildschut HIJ, Brandenburg H, den Hollander NS, Schoonderwaldt EM, Pijpers L, Galjaard RJH, Van Opstal D (2001). The diagnostic performance of cytogenetic investigation in amniotic fluid cells and chorionic villi. Prenat Diagn 21: 1150-1158.

Den Hollander NS, Wessels MW, Niermeijer MF, Los FJ, Wladimiroff JW (2002). Early fetal anomaly scanning in a population at increased risk of abnormalities. Ultrasound Obstet Gynecol 19: 570-574.

Wessels MW, Los FJ, Frohn-Mulder IME, Niermeijer MF, Willems PJ, Wladimiroff JW (2003). Poor outcome in Down syndrome fetuses with cardiac anomalies or growth retardation. Am J Med Genet 116A: 147-151.

Wladimiroff JW, Cohen-Overbeek TE, Ursem NTC, Bijma H, Los FJ (2003). Geavanceerd ultrageluidonderzoek naar aangeboren afwijkingen in Rotterdam; 20 jaar ervaring. Ned Tijdschr Geneeskd 147: 2106-2110.

Los FJ, Van Opstal D, van den Berg C (2004). The development of cytogenetically normal, abnormal and mosaic embryos: a theoretical model. Hum Reprod Update 10: 79-94.

Baart EB, Van Opstal D, Los FJ, Fauser BCJM, Martini E (2004). Fluorescence in situ hybridization analysis of two blastomeres from day 3 frozen-thawed embryos followed by analysis of the remaining embryo on day 5. Hum Reprod 19: 685-693.

Kleijer WJ, van den Berg P, Los FJ (2004). Prenatal diagnosis of Lesch-Nyhan disease. Prenat Diagn 24: 658-659.

Jacobs LJAM, de Coo IFM, Nijland JG, Galjaard RJH, Los FJ, Schoonderwoerd K, Niermeijer MF, Geraedts JPM, Scholte HR, Smeets HJM (2005). Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation. Mol Hum Reprod 11: 223-228.

Huizinga-Arp CRC, Los FJ, van der Laan JW (2008). Zwanger en rinitis: lokale corticosteroiden. Pharmaceutisch Weekblad  143: 44-45.

Als lid van de Wetenschappelijke Raad Medicatiebewaking. (2008). Commentaren Medicatiebewaking 2008/2009. Houten: Health Base.

Los FJ (2010). De toestand in de baarmoeder. Het prenataal onderzoek van de foetus. Sleeuwijk: eigen uitgave.