| | Title | Authors / Editors | Date |
|
unige:9213 |
Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3 |
Lasseter, V. K.; Pulver, A. E.; Wolyniec, P. S.; Nestadt, G.; ... Kasch, L. |
1995 |
|
unige:8862 |
Schizophrenia and chromosomal deletions within 22q11.2 |
Lindsay, E. A.; Morris, Michael Andréw; Gos, A.; Nestadt, G.; ... Pulver, A. E. |
1995 |
|
unige:8746 |
Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients |
Fokstuen, Siv; Bottani, Armand; Medeiros, P. F.; Antonarakis, Stylianos; ... Schinzel, A. |
1997 |
|
unige:8681 |
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y |
Chen, H.; Rossier, Colette; Morris, Michael Andréw; Scott, Hamish Steele; ... Antonarakis, Stylianos |
1999 |
|
unige:8734 |
Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study |
Eliez, Stéphan; Antonarakis, Stylianos; Morris, Michael Andréw; Dahoun, S. P.; Reiss, A. L. |
2001 |
|
unige:8758 |
Language skills in children with velocardiofacial syndrome (deletion 22q11.2) |
Glaser, Bronwyn; Mumme, D. L.; Blasey, Christine; Morris, Michael Andréw; ... Eliez, Stéphan |
2002 |
|
unige:8725 |
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome |
Deutsch, Samuel; Rideau, Alexandra; Bochaton-Piallat, Marie-Luce; Merla, Giuseppe; ... Beris, Photis |
2003 |
Chromosomes, human, pair 22/ genetics
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