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Risk of erroneous results in carrier testing for haemophilia A without prior DNA analysis in male index patients. [electronic resource] by
- Fransen van de Putte, D E
- Frankhuizen, W S
- Vijfhuizen, L
- Groenewegen, L
- Tamminga, R Y J
- Bouman, K
- van Essen, A J
- Gijsbers, A C J
- Ruivenkamp, C A L
- Boon, E M J
Producer: 20160118
In:
Haemophilia : the official journal of the World Federation of Hemophilia vol. 21
Availability: No items available.
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11.
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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. [electronic resource] by
- Bijlsma, E K
- Gijsbers, A C J
- Schuurs-Hoeijmakers, J H M
- van Haeringen, A
- Fransen van de Putte, D E
- Anderlid, B-M
- Lundin, J
- Lapunzina, P
- Pérez Jurado, L A
- Delle Chiaie, B
- Loeys, B
- Menten, B
- Oostra, A
- Verhelst, H
- Amor, D J
- Bruno, D L
- van Essen, A J
- Hordijk, R
- Sikkema-Raddatz, B
- Verbruggen, K T
- Jongmans, M C J
- Pfundt, R
- Reeser, H M
- Breuning, M H
- Ruivenkamp, C A L
Producer: 20090901
In:
European journal of medical genetics vol. 52
Availability: No items available.
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