The following pages link to 1p36 deletion syndrome
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Asymmetric crying facies (links | edit)
- List of ICD-9 codes 740–759: congenital anomalies (links | edit)
- XX male syndrome (links | edit)
- XXYY syndrome (links | edit)
- Monosomy 9p (links | edit)
- Pallister–Killian syndrome (links | edit)
- List of diseases (0–9) (links | edit)
- XXXXY syndrome (links | edit)
- Diffuse large B-cell lymphoma (links | edit)
- XX gonadal dysgenesis (links | edit)
- Gonadal dysgenesis (links | edit)
- 22q13 deletion syndrome (links | edit)
- Chromosome abnormality (links | edit)
- Ring chromosome 20 syndrome (links | edit)
- 1p36 Deletion Syndrome (redirect page) (links | edit)
- Marker chromosome (links | edit)
- Acute myeloblastic leukemia with maturation (links | edit)
- Confined placental mosaicism (links | edit)
- Ewing sarcoma (links | edit)
- Cat eye syndrome (links | edit)
- Trisomy 22 (links | edit)
- Chromosomal rearrangement (links | edit)
- Alveolar rhabdomyosarcoma (links | edit)
- Mantle cell lymphoma (links | edit)
- Trisomy 16 (links | edit)
- Acute megakaryoblastic leukemia (links | edit)
- Chromosome 1, 1p36 deletion syndrome (redirect page) (links | edit)
- List of diseases (C) (links | edit)
- Talk:Chromosome 1, 1p36 deletion syndrome (transclusion) (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive7 (links | edit)
- User:AlexNewArtBot/ChemistrySearchResult/archive11 (links | edit)
- User:AlexNewArtBot/TestFeedSearchResult/archive42 (links | edit)
- User:B. Wolterding/Merge by project/Page 1 (links | edit)
- User talk:Anandks007/Med (links | edit)
- 2p15-16.1 microdeletion syndrome (links | edit)
- Monosomy 1p36 syndrome (redirect page) (links | edit)
- Monosomy 1p36 (redirect page) (links | edit)
- Angelman syndrome (links | edit)
- Cingulin-like protein 1 (links | edit)
- Klinefelter syndrome (links | edit)
- Tetrasomy (links | edit)
- Tetrasomy 9p (links | edit)
- Myxoid liposarcoma (links | edit)
- T(11:14) (links | edit)
- Monosomy 14 (links | edit)
- Roberts syndrome (links | edit)
- Koolen–De Vries syndrome (links | edit)
- 3q29 microdeletion syndrome (links | edit)
- 1q21.1 deletion syndrome (links | edit)
- 1q21.1 duplication syndrome (links | edit)
- 2q37 monosomy (links | edit)
- 22q11.2 duplication syndrome (links | edit)
- Proximal 18q- (links | edit)
- DbCRID (links | edit)
- Distal 18q- (links | edit)
- Ring chromosome 18 (links | edit)
- 46,XX/46,XY (links | edit)