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A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11. [electronic resource] by
- Stuppia, L
- Gatta, V
- Calabrese, G
- Guanciali Franchi, P
- Morizio, E
- Bombieri, C
- Mingarelli, R
- Sforza, V
- Frajese, G
- Tenaglia, R
- Palka, G
Producer: 19980716
In:
Human genetics vol. 102
Availability: No items available.
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12152.
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12153.
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Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay. [electronic resource] by
- Upadhyaya, M
- Ruggieri, M
- Maynard, J
- Osborn, M
- Hartog, C
- Mudd, S
- Penttinen, M
- Cordeiro, I
- Ponder, M
- Ponder, B A
- Krawczak, M
- Cooper, D N
Producer: 19980716
In:
Human genetics vol. 102
Availability: No items available.
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[Incidence of psychiatric symptoms and somatic complaints in 4- to 10-year-old children in Germany as judged by parents--a comparison of norm-oriented and criteria-oriented models]. [electronic resource] by
- Lehmkuhl, G
- Döpfner, M
- Plück, J
- Berner, W
- Fegert, J M
- Huss, M
- Lenz, K
- Schmeck, K
- Lehmkuhl, U
- Poustka, F
Producer: 19980831
In:
Zeitschrift fur Kinder- und Jugendpsychiatrie und Psychotherapie vol. 26
Availability: No items available.
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12160.
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