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1
Sex-linked mental retardation
Sex-linked mental retardation
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Sex-linked mental retardation

Hamel, B C ; Poppelaars, F A

Nederlands tijdschrift voor geneeskunde, 2000-09, Vol.144 (36), p.1713-1716

Netherlands

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2
Fluorescence in situ hybridization in the study of chromosomal abnormalities
Fluorescence in situ hybridization in the study of chromosomal abnormalities
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Fluorescence in situ hybridization in the study of chromosomal abnormalities

Hoovers, J M ; Mellink, C H ; Leschot, N J

Nederlands tijdschrift voor geneeskunde, 1999-11, Vol.143 (45), p.2265-2268

Netherlands

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3
Chromosomal deviations in subfertile men and their partners is often not a reason to refrain from intracytoplasmic sperm injection
Chromosomal deviations in subfertile men and their partners is often not a reason to refrain from intracytoplasmic sperm injection
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Chromosomal deviations in subfertile men and their partners is often not a reason to refrain from intracytoplasmic sperm injection

Gebhardt, D O

Nederlands tijdschrift voor geneeskunde, 1999-09, Vol.143 (37), p.1893-1894

Netherlands

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4
Trisomy 9p: a clinical picture and the importance of examining the family
Trisomy 9p: a clinical picture and the importance of examining the family
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Trisomy 9p: a clinical picture and the importance of examining the family

van Ravenswaaij-Arts, C ; van der Looij, E ; Smeets, D

Nederlands tijdschrift voor geneeskunde, 1999-03, Vol.143 (13), p.682-686

Netherlands

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5
Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities
Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities
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Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities

Boormans, E M A ; van Lith, J M M ; Bilardo, C M ; Knegt, A C ; Oepkes, D ; Hoffer, M J V ; Boon, E M J ; Wildschut, H I J ; Galjaard, R J H ; Schuring-Blom, G H ; van Oppen, A C C ; Smits, A ; Creemers, J ; Go, A ; Nieuwint, A ; Nijhuis, J G ; de Die, C ; Bonsel, G J ; Birnie, E ; Leschot, N

Nederlands tijdschrift voor geneeskunde, 2006-11, Vol.150 (44), p.2455; author reply 2455-2455; author reply 2455

Netherlands

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6
Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping
Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping
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Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping

Scholtes, M C W

Nederlands tijdschrift voor geneeskunde, 2007-10, Vol.151 (42), p.2350; author reply 2350-2350; author reply 2351

Netherlands

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7
Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities
Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities
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Rapid prenatal diagnosis of chromosomal abnormalities; limitations and possibilities

van Zwieten, M C B ; Leschot, N J ; Willems, D L

Nederlands tijdschrift voor geneeskunde, 2006-11, Vol.150 (44), p.2454; author reply 2454-2454; author reply 2454

Netherlands

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8
Examples of preimplantation genetic diagnosis versus prenatal diagnosis in carriers of genetic abnormalities: advantages and disadvantages
Examples of preimplantation genetic diagnosis versus prenatal diagnosis in carriers of genetic abnormalities: advantages and disadvantages
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Examples of preimplantation genetic diagnosis versus prenatal diagnosis in carriers of genetic abnormalities: advantages and disadvantages

Snel, B J ; Ypma, T D

Nederlands tijdschrift voor geneeskunde, 2008-03, Vol.152 (13), p.768-771

Netherlands

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9
Sonomarkers: subtle ultrasound findings in the 20-week ultrasound examination, which have a low association with some chromosomal and non-chromosomal abnormalities in the fetus
Sonomarkers: subtle ultrasound findings in the 20-week ultrasound examination, which have a low association with some chromosomal and non-chromosomal abnormalities in the fetus
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Sonomarkers: subtle ultrasound findings in the 20-week ultrasound examination, which have a low association with some chromosomal and non-chromosomal abnormalities in the fetus

Grijseels, E W M ; Cohen-Overbeek, T E ; Adama van Scheltema, P N ; Groenenberg, I A L ; Schoonderwaldt, E M ; Steegers, E A P ; Wildschut, H I J

Nederlands tijdschrift voor geneeskunde, 2008-10, Vol.152 (41), p.2225-2231

Netherlands

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10
Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping
Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping
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Risk factors for structural chromosomal abnormality in > or = 2 miscarriages, as an instrument for selective karyotyping

Vlaanderen, W

Nederlands tijdschrift voor geneeskunde, 2007-10, Vol.151 (42), p.2351; author reply 2351-2351; author reply 2352

Netherlands

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