Molecular Basis of Congenital Glaucoma - 8 Angebote vergleichen
| Preise | 2018 | 2019 | 2020 | 2022 |
|---|---|---|---|---|
| Schnitt | Fr. 45.90 (€ 46.95)¹ | Fr. 46.83 (€ 47.90)¹ | Fr. 49.15 (€ 50.27)¹ | Fr. 48.87 (€ 49.99)¹ |
| Nachfrage |
1
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Molecular Basis of Congenital Glaucoma (2018)
~EN PB NWISBN: 9783330062832 bzw. 3330062835, vermutlich in Englisch, LAP Lambert Academic Publishing Mai 2018, Taschenbuch, neu.
Von Händler/Antiquariat, BuchWeltWeit Inh. Ludwig Meier e.K. [57449362], Bergisch Gladbach, Germany.
Neuware - A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics. 112 pp. Englisch.
Neuware - A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics. 112 pp. Englisch.
2
Molecular Basis of Congenital Glaucoma
~EN NW ABISBN: 9783330062832 bzw. 3330062835, vermutlich in Englisch, neu, Hörbuch.
Lieferung aus: Österreich, Lieferzeit: 5 Tage, zzgl. Versandkosten.
A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics.
A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics.
3
Symbolbild
Molecular Basis of Congenital Glaucoma (2018)
~EN PB NWISBN: 9783330062832 bzw. 3330062835, vermutlich in Englisch, 112 Seiten, LAP Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Free shipping.
Von Händler/Antiquariat, Buchhandlung Kisch & Co. [3338288].
Neuware - A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics. 15.05.2018, Taschenbuch, Neuware, 220x150x7 mm, 183g, 112, Internationaler Versand, Offene Rechnung (Vorkasse vorbehalten), PayPal, Banküberweisung.
Von Händler/Antiquariat, Buchhandlung Kisch & Co. [3338288].
Neuware - A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics. 15.05.2018, Taschenbuch, Neuware, 220x150x7 mm, 183g, 112, Internationaler Versand, Offene Rechnung (Vorkasse vorbehalten), PayPal, Banküberweisung.
4
Symbolbild
Molecular Basis of Congenital Glaucoma (2018)
~EN PB NWISBN: 9783330062832 bzw. 3330062835, vermutlich in Englisch, 112 Seiten, LAP Lambert Academic Publishing, Taschenbuch, neu.
Von Händler/Antiquariat, Rheinberg-Buch, [3813847].
Neuware - A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics. 15.05.2018, Taschenbuch, Neuware, 220x150x7 mm, 183g, 112, Internationaler Versand, PayPal, Offene Rechnung, Banküberweisung, Sofortüberweisung.
Neuware - A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics. 15.05.2018, Taschenbuch, Neuware, 220x150x7 mm, 183g, 112, Internationaler Versand, PayPal, Offene Rechnung, Banküberweisung, Sofortüberweisung.
5
Molecular Basis of Congenital Glaucoma (2018)
EN PB NWISBN: 9783330062832 bzw. 3330062835, in Englisch, LAP Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Vereinigtes Königreich Grossbritannien und Nordirland, Usually dispatched within 4 to 5 days. real shipping costs can differ.
Von Händler/Antiquariat, Book Depository.
LAP Lambert Academic Publishing, Paperback, Published: 2018-05-15T00:00:01Z, Product group: Book.
Von Händler/Antiquariat, Book Depository.
LAP Lambert Academic Publishing, Paperback, Published: 2018-05-15T00:00:01Z, Product group: Book.
6
Molecular Basis of Congenital Glaucoma
DE PB NWISBN: 9783330062832 bzw. 3330062835, in Deutsch, LAP LAMBERT Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei, Shipping in 3 days.
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
7
Molecular Basis of Congenital Glaucoma
EN PB NWISBN: 9783330062832 bzw. 3330062835, in Englisch, Taschenbuch, neu.
New from: CDN$ 77.09 (4 Offers)
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Lieferung aus: Kanada, Usually ships within 4 to 5 days. real shipping costs can differ.
Von Händler/Antiquariat, Book Depository CA.
Paperback, Product group: Book.
Von Händler/Antiquariat, Book Depository CA.
Paperback, Product group: Book.
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