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A strategy to reveal high-frequency RFLPs along the human X chromosome. [electronic resource] by
- Aldridge, J
- Kunkel, L
- Bruns, G
- Tantravahi, U
- Lalande, M
- Brewster, T
- Moreau, E
- Wilson, M
- Bromley, W
- Roderick, T
Producer: 19840719
In:
American journal of human genetics vol. 36
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125.
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126.
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DNA-based detection of chromosome deletion and amplification: diagnostic and mechanistic significance. [electronic resource] by
- Latt, S A
- Lalande, M
- Donlon, T
- Wyman, A
- Rose, E
- Shiloh, Y
- Korf, B
- Müller, U
- Sakai, K
- Kanda, N
Producer: 19870626
In:
Cold Spring Harbor symposia on quantitative biology vol. 51 Pt 1
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128.
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Isolation of DNA sequences on human chromosome 21 by application of a recombination-based assay to DNA from flow-sorted chromosomes. [electronic resource] by
- Tantravahi, U
- Stewart, G D
- Van Keuren, M
- McNeil, G
- Roy, S
- Patterson, D
- Drabkin, H
- Lalande, M
- Kurnit, D M
- Latt, S A
Producer: 19880914
In:
Human genetics vol. 79
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135.
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Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients. [electronic resource] by
- Moncla, A
- Malzac, P
- Voelckel, M A
- Auquier, P
- Girardot, L
- Mattei, M G
- Philip, N
- Mattei, J F
- Lalande, M
- Livet, M O
Producer: 19990615
In:
European journal of human genetics : EJHG vol. 7
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136.
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137.
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Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia. [electronic resource] by
- Latt, S A
- Kaiser, T N
- Lojewski, A
- Dougherty, C
- Juergens, L
- Brefach, S
- Sahar, E
- Gustashaw, K
- Schreck, R R
- Powers, M
- Lalande, M
Producer: 19821202
In:
Cytogenetics and cell genetics vol. 33
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138.
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Molecular genetic approaches to human diseases involving mental retardation. [electronic resource] by
- Latt, S A
- Kurnit, D M
- Bruns, G P
- Schreck, R R
- Morton, C C
- Kunkel, L M
- Lalande, M
- Aldridge, J
- Neve, R
- Tantravahi, U
Producer: 19840719
In:
American journal of mental deficiency vol. 88
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139.
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A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus. [electronic resource] by
- Nakatsu, Y
- Tyndale, R F
- DeLorey, T M
- Durham-Pierre, D
- Gardner, J M
- McDanel, H J
- Nguyen, Q
- Wagstaff, J
- Lalande, M
- Sikela, J M
Producer: 19930816
In:
Nature vol. 364
Availability: No items available.
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140.
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The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. [electronic resource] by
- Jay, P
- Rougeulle, C
- Massacrier, A
- Moncla, A
- Mattei, M G
- Malzac, P
- Roëckel, N
- Taviaux, S
- Lefranc, J L
- Cau, P
- Berta, P
- Lalande, M
- Muscatelli, F
Producer: 19971204
In:
Nature genetics vol. 17
Availability: No items available.
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