scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1651-2227.1976.TB04923.X |
P698 | PubMed publication ID | 937003 |
P2093 | author name string | Akerblom HK | |
Koivisto M | |||
de La Chapelle A | |||
Remes M | |||
P2860 | cites work | Use of activated charcoal in the radioimmunoassay of human growth hormone in plasma | Q36551184 |
RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISM | Q41939552 | ||
P433 | issue | 4 | |
P921 | main subject | karyotype | Q189967 |
growth hormone deficiency | Q369262 | ||
P304 | page(s) | 513-518 | |
P577 | publication date | 1976-07-01 | |
P1433 | published in | Acta Paediatrica Scandinavica | Q27708772 |
P1476 | title | Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32). | |
P478 | volume | 65 |
Q34468912 | A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency. |
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Q68586990 | Cytogenetic analysis in congenital hypothyroidism |
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Q33584670 | De novo interstitial deletion del(1)(p21p32) |
Q72108918 | Immune function in patients with chromosome deletions |
Q51945810 | Interstitial 1q25.3‐q31.3 deletion in a boy with mild manifestations |
Q41847533 | Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter). |
Q41932489 | Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence |
Q35202320 | Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus |
Q41936487 | Terminal deletion of the long arm of chromosome 1 in a malformed newborn |
Q41684207 | Terminal long-arm deletion of chromosome 1 in a male infant |
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